Dihydrolevoglucosenone

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Dihydrolevoglucosenone
Dihydrolevoglucosenone.svg
Names
IUPAC name
(1R)-7,8-Dioxabicyclo[3.2.1]octan-2-one
Other names
Cyrene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.234.612 Edit this at Wikidata
EC Number
  • 807-130-4
Properties
C6H8O3
Molar mass 128.127 g·mol−1
Appearance clear to yellowish liquid
Density 1.2508 g/cm3 (20 °C) [1]
Boiling point 226 °C (439 °F; 499 K) [1]
miscible
Vapor pressure 14.4 Pa (25 °C) [1]
1.4732 (20 °C) [1]
Hazards[2]
GHS pictograms GHS07: Harmful
GHS Signal word Warning
GHS hazard statements
 H319
P305+351+338, P313
Flash point 108 °C (226 °F; 381 K)
296 °C (565 °F; 569 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dihydrolevoglucosenone (Cyrene) is a bicyclic, chiral, seven-membered heterocyclic cycloalkanone which is a waste derived and fully biodegradable aprotic dipolar solvent.[3][4][5] It is a environmentally friendly alternative to dimethylformamide (DMF) and N-methyl-2-pyrrolidone (NMP).[6]

Preparation[]

Acidic pyrolysis of cellulose to yield levoglucosenone (LGO)

Dihydrolevoglucosenone can be prepared through the hydrogenation of unsaturated ketone levoglucosenone (LGO) with heterogenous palladium catalysts under mild conditions.[7][8] LGO is a chemical building block obtained by acid-catalyzed pyrolysis[9] of lignocellulosic biomass such as sawdust.

Properties[]

Dihydrolevoglucosenone is a clear colorless, to light-yellow liquid with a mild, smoky ketone-like odor.[10] It is miscible with water and many organic solvents.[10] Dihydrolevoglucosenone has a boiling point of 226 °C at 101.325 kPa (vs 202 °C for NMP), and a vapor pressure of 14.4 Pa near room temperature (25  °C).[1] It has a comparatively high dynamic viscosity of 14.5 cP (for comparison DMF: 0.92 cP at 20 °C, NMP: 1.67 cP at 25 °C).[11]

The compound is stable at temperatures up to 195 °C and weak acids and bases.[citation needed] Dihydrolevoglucosenone can react with inorganic bases via an aldol condensation mechanism.[citation needed] Dihydrolevoglucosenone is readily biodegradable (99% within 14 days) and reacts to oxidants such as aqueous 30% hydrogen peroxide solution even at room temperature.[citation needed]

Applications[]

Hydrogenation of LGO zu tetrahydrofuran-2,5-dimethanol

Dihydroglucosenone as a precursor[]

Formation of hydroxymethyl-butyrolactone

Dihydrolevoglucosenone can be used as a renewable building block to produce a number of higher value chemicals such as drugs, flavours and fragrances and specialty polymers.[7]

The oxidation of dihydrolevoglucosenone with peracids such as peracetic acid in acetic acid produces optically pure 5-hydroxymethyldihydrofuranone [(S) - (+) - 4-hydroxymethyl-γ-butyrolactone],[12] from which zalcitabine (2'-3'-dideoxycytidine, ddC), formerly a HIV drug, is available.[13]

In a two-step hydrogenation process with a metal catalyst – first at 60 °C then at 180 °C – 1,6-hexanediol is mainly obtained via several intermediates.[14] 1,6-hexanediol can be used as a starting material for the production of polyesters, polyurethanes and diamine 1,6-diaminohexane.

At elevated temperature and in the presence of a palladium catalyst, hydrogenolysis of dihydrolevoglucosenone via levoglucosanol selectively yields tetrahydrofuran-2,5-dimethanol (THF-dimethanol),[7] which is a biodegradable solvent and a bio-based precursor to 1,6-hexanediol (and 1,6-diaminohexane).[15]

Dihydroglucosenone as a safer solvent[]

Formation of ureas using dihydrolevoglucosenone as a solvent

The search for alternative "green" solvents made from biomass or low-cost renewable raw materials, which are accessible through high-efficiency processes, in high yields, and meet the performance of conventional solvents,[16] has triggered intensive research activities in industry and academia worldwide.

Dihydrolevoglucosenone is considered a "green" replacement for DMF.[4] Several standard reactions of organic chemistry, e.g. Menshutkin reaction,[4] Sonogashira coupling,[17] Suzuki-Miyaura coupling[18] and the production of ureas[19] have been carried out in dihydrolevoglucosenone.

Production[]

Circa Group produces dihydrolevoglucosenone from cellulose under the Cyrene brand and has built a 50-tonne demonstration plant with partners in Tasmania. The company estimates that dihydroglucosenone performs better than NMP in 45% and comparably to NMP in 20% of trials to date. Circa received authorization in 2018 from the European Chemicals Agency (ECHA) to produce or import up to 100 tonnes per year of dihydroglucosenone to the EU.[20]

Literature[]

  • DS van Es: Study into alternative (biobased) polar aprotic solvents. Wageningen University, Wageningen 2017 (wur.nl [PDF]).
  • JH Clark, A. Hunt, C. Topi, G. Paggiola, J. Sherwood: Sustainable Solvents: Perspectives from Research, Business and Institutional Policy . Royal Society of Chemistry, London 2017, ISBN 978-1-78262-335-9 .

References[]

  1. ^ Jump up to: a b c d e Baird, Zachariah Steven; Uusi-Kyyny, Petri; Pokki, Juha-Pekka; Pedegert, Emilie; Alopaeus, Ville (6 Nov 2019). "Vapor Pressures, Densities, and PC-SAFT Parameters for 11 Bio-compounds". International Journal of Thermophysics. 40 (11): 102. Bibcode:2019IJT....40..102B. doi:10.1007/s10765-019-2570-9.
  2. ^ Circa Group (23 January 2017). "Safety Data Sheet" (PDF).
  3. ^ "Concise and Efficient Synthesis of E-stereoisomers of exo-cyclic Carbohydrate Enones. Aldol Condensation of Dihydrolevoglucosenone with Five-membered Aromatic Aldehydes1 Part 1. - PubAg". pubag.nal.usda.gov. US: United States National Agricultural Library, USA.gov. Retrieved 2019-01-31.
  4. ^ Jump up to: a b c Sherwood, James; De bruyn, Mario; Constantinou, Andri; Moity, Laurianne; McElroy, C. Rob; Farmer, Thomas J.; Duncan, Tony; Raverty, Warwick; Hunt, Andrew J. (2014-09-04). "Dihydrolevoglucosenone (Cyrene) as a bio-based alternative for dipolar aprotic solvents". Chem. Commun. 50 (68): 9650–9652. doi:10.1039/c4cc04133j. PMID 25007289.
  5. ^ "(1S,5R)-6,8-dioxabicyclo[3.2.1]octan-4-one - Registration Dossier - ECHA". echa.europa.eu. European Chemicals Agency, Europa (web portal). Retrieved 2019-01-31.
  6. ^ Clark, James H.; Hunt, Andrew J.; Raverty, Warwick; Duncan, Tony; Farmer, Thomas J.; McElroy, C. Rob; Moity, Laurianne; Constantinou, Andri; Bruyn, Mario De (2014-07-29). "Dihydrolevoglucosenone (Cyrene) as a bio-based alternative for dipolar aprotic solvents". Chemical Communications. 50 (68): 9650–9652. doi:10.1039/C4CC04133J. ISSN 1364-548X. PMID 25007289.
  7. ^ Jump up to: a b c Huber, George W.; Dumesic, James A.; Rashke, Quinn A.; McClelland, Daniel J.; Krishna, Siddarth H. (2017-03-06). "Hydrogenation of levoglucosenone to renewable chemicals". Green Chemistry. 19 (5): 1278–1285. doi:10.1039/C6GC03028A. ISSN 1463-9270. OSTI 1477850.
  8. ^ Mazarío, Jaime; Parreño Romero, Míriam; Concepción, Patricia; Chávez-Sifontes, Marvin; Spanevello, Rolando A.; Comba, María B.; Suárez, Alejandra G.; Domine, Marcelo E. (2019-07-26). "Tuning zirconia-supported metal catalysts for selective one-step hydrogenation of levoglucosenone". Green Chemistry. 21 (17): 4769–4785. doi:10.1039/C9GC01857C. hdl:11336/108039. ISSN 1463-9270.
  9. ^ Trahanovsky; et al. (December 5, 2002). "A Convenient Procedure for the Preparation of Levoglucosenone and Its Conversion to Novel Chiral Derivatives". Carbohydrate Synthons in Natural Products Chemistry. ACS Symposium Series. 841. pp. 21–31. doi:10.1021/bk-2003-0841.ch002. ISBN 978-0-8412-3740-7.
  10. ^ Jump up to: a b "Circa Data Sheet" (PDF). Archived (PDF) from the original on 2018-01-09.
  11. ^ Shuttleworth, P. S.; Clark, J. H.; Ellis, G. J.; Budarin, V. L.; Bruyn, M. De; Sherwood, J.; Salavagione, H. J. (2017-06-06). "Identification of high performance solvents for the sustainable processing of graphene" (PDF). Green Chemistry. 19 (11): 2550–2560. doi:10.1039/C7GC00112F. ISSN 1463-9270.
  12. ^ Method of producing (S)-4-hydroxymethyl-γ-lactone, 1990-09-17, retrieved 2019-01-31
  13. ^ Okabe, Masami; Sun, Ruen Chu; Tam, Steve Y. K.; Todaro, Louis J.; Coffen, David L. (2002-05-01). "Synthesis of the dideoxynucleosides "ddC" and "CNT" from glutamic acid, ribonolactone, and pyrimidine bases". The Journal of Organic Chemistry. 53 (20): 4780–4786. doi:10.1021/jo00255a021.
  14. ^ Process for preparing 1,6-hexanediol, 2013-04-25, retrieved 2019-01-31
  15. ^ Huber, George W.; Dumesic, James A.; Hermans, Ive; Maravelias, Christos T.; Banholzer, Williams F.; Walker, Theodore; Burt, Samuel P.; Brentzel, Zachary J.; Alonso, David M. (2017-09-20). "New catalytic strategies for α,ω-diols production from lignocellulosic biomass". Faraday Discussions. 202: 247–267. Bibcode:2017FaDi..202..247H. doi:10.1039/C7FD00036G. ISSN 1364-5498. PMID 28678237. S2CID 39560658.
  16. ^ Byrne, Fergal P.; Jin, Saimeng; Paggiola, Giulia; Petchey, Tabitha H. M.; Clark, James H.; Farmer, Thomas J.; Hunt, Andrew J.; Robert McElroy, C.; Sherwood, James (2016-05-23). "Tools and techniques for solvent selection: green solvent selection guides". Sustainable Chemical Processes. 4 (1): 7. doi:10.1186/s40508-016-0051-z. ISSN 2043-7129.
  17. ^ Watson, Allan J. B.; Jamieson, Craig; Greatrex, Ben; Murray, Jane; Kennedy, Alan R.; Wilson, Kirsty L. (2016-09-08). "Scope and limitations of a DMF bio-alternative within Sonogashira cross-coupling and Cacchi-type annulation". Beilstein Journal of Organic Chemistry. 12 (1): 2005–2011. doi:10.3762/bjoc.12.187. ISSN 1860-5397. PMC 5082449. PMID 27829904.
  18. ^ Watson, Allan J. B.; Jamieson, Craig; Murray, Jane; Wilson, Kirsty L. (2017-12-11). "Cyrene as a Bio-Based Solvent for the Suzuki–Miyaura Cross-Coupling". Synlett. 29 (5): 650–654. doi:10.1055/s-0036-1589143. ISSN 0936-5214.
  19. ^ Camp, Jason E.; Bousfield, Thomas W.; Mapesa, Kopano; Mistry, Liam (2017-05-08). "Synthesis of ureas in the bio-alternative solvent Cyrene" (PDF). Green Chemistry. 19 (9): 2123–2128. doi:10.1039/C7GC00908A. ISSN 1463-9270.
  20. ^ Gyekye, Liz. "Circa gets thumbs up from EU to sell its bio-based solvent in the bloc". www.biobasedworldnews.com. Archived from the original on 2019-01-05. Retrieved 2019-01-31.
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