Pivalic acid

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Pivalic acid
Pivalic acid.svg
Pivalic-acid-3D-balls.png
Names
Preferred IUPAC name
2,2-Dimethylpropanoic acid
Other names
Pivalic acid
Dimethylpropanoic acid
Neopentanoic acid
Trimethylacetic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.839 Edit this at Wikidata
UNII
  • InChI=1S/C5H10O2/c1-5(2,3)4(6)7/h1-3H3,(H,6,7) checkY
    Key: IUGYQRQAERSCNH-UHFFFAOYSA-N checkY
  • O=C(O)C(C)(C)C
Properties
C5H10O2
Molar mass 102.133 g·mol−1
Density 0.905 g/cm3
Melting point 35 °C (95 °F; 308 K)
Boiling point 163.7 °C (326.7 °F; 436.8 K)
Related compounds
Related compounds
 neopentyl alcohol
neopentane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY  (what is checkY☒N ?)
Infobox references

Pivalic acid is a carboxylic acid with a molecular formula of (CH3)3CCO2H. This colourless, odiferous organic compound is solid at room temperature. A common abbreviation for the pivalyl or pivaloyl group (t-BuC(O)) is Piv and for pivalic acid (t-BuC(O)OH) is PivOH.

Preparation[]

Industrial route[]

Pivalic acid is prepared by hydrocarboxylation of isobutene via the Koch reaction:

(CH3)2C=CH2 + CO + H2O → (CH3)3CCO2H

Such reactions require an acid catalyst such as hydrogen fluoride. tert-Butyl alcohol and isobutyl alcohol can also be used in place of isobutene. Globally, several million kilograms are produced annually.[1] Pivalic acid is also economically recovered as a byproduct from the production of semisynthetic penicillins like ampicillin and amoxycillin.

Laboratory methods[]

It was originally prepared by the oxidation of pinacolone with chromic acid[2] and by the hydrolysis of tert-butyl cyanide.[3] Convenient laboratory routes proceed via tert-butyl chloride via carbonation of the Grignard reagent[4] and by oxidation of pinacolone.[5]

Pinacol rearrangement
t-Butylmagnesium bromide reacts with CO2 to form the pivalate salt. Addition of acid yields pivalic acid

Applications[]

Relative to esters of most carboxylic acids, esters of pivalic acid are unusually resistant to hydrolysis. Some applications result from this thermal stability. Polymers derived from pivalate esters of vinyl alcohol are highly reflective lacquers. The pivaloyl (abbreviated Piv or Pv) group is a protective group for alcohols in organic synthesis. Pivalic acid is sometimes used as an internal chemical shift standard for NMR spectra of aqueous solutions. While DSS is more commonly used for this purpose, the minor peaks from protons on the three methylene bridges in DSS can be problematic. The 1H NMR spectrum at 25 °C and neutral pH is a singlet at 1.08 ppm. Pivalic acid is employed as co-catalyst in some of the Palladium catalyzed C-H functionalization reaction.[6][7]

Alcohol protection[]

The pivaloyl group is used as a protecting group in organic synthesis. Common protection methods include treatment of alcohol with pivaloyl chloride (PvCl) in presence of pyridine.[8]

PvProtectedAlcohol.png

Alternatively, the esters can be prepared using pivaloic anhydride in the presence of scandium triflate (Sc(OTf)3) or (VO(OTf)2).

Common deprotection methods involve hydrolysis with a base or other nucleophiles.[9][10][11][12]

PvProtection.png

See also[]

References[]

  1. ^ Riemenschneider, Wilhelm (2000). "Carboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a05_235. ISBN 3527306730.
  2. ^ Friedel and Silva, Ber. 6, 146, 826 (1873).[full citation needed]
  3. ^ Butlerow, Ann. 165, 322 (1873).[full citation needed]
  4. ^ S. V. Puntambeker; E. A. Zoellner; L. T. Sandborn; E. W. Bousquet (1941). "Trimethylacetic acid from tert.- Butyl Chloride". Organic Syntheses. doi:10.15227/orgsyn.008.0104.; Collective Volume, 1, p. 524
  5. ^ L. T. Sandborn; E. W. Bousquet (1941). "Trimethylacetic acid from Pinacolone". Organic Syntheses. doi:10.15227/orgsyn.008.0104.; Collective Volume, 1, p. 524
  6. ^ Lafrance, Marc; Fagnou, Keith (2006-12-27). "Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design". Journal of the American Chemical Society. 128 (51): 16496–16497. doi:10.1021/ja067144j. ISSN 0002-7863. PMID 17177387.
  7. ^ Zhao, Dongbing; Wang, Weida; Lian, Shuang; Yang, Fei; Lan, Jingbo; You, Jingsong (2009-01-26). "Phosphine-Free, Palladium-Catalyzed Arylation of Heterocycles through CH Bond Activation with Pivalic Acid as a Cocatalyst". Chemistry – A European Journal. 15 (6): 1337–1340. doi:10.1002/chem.200802001. ISSN 0947-6539.
  8. ^ Robins, Morris J.; Hawrelak, S. D.; Kanai, Tadashi; Siefert, Jan Marcus; Mengel, Rudolf (1979). "Nucleic acid related compounds. 30. Transformations of adenosine to the first 2',3'-aziridine-fused nucleosides, 9-(2,3-epimino-2,3-dideoxy-.beta.-D-ribofuranosyl)adenine and 9-(2,3-epimino-2,3-dideoxy-.beta.-D-lyxofuranosyl)adenine". The Journal of Organic Chemistry. 44 (8): 1317–22. doi:10.1021/jo01322a026.
  9. ^ Van Boeckel, C.A.A.; Van Boom, J.H. (1979). "Synthesis of glucosylphosphatidylglycerol via a phosphotriester intermediate". Tetrahedron Letters. 20 (37): 3561–4. doi:10.1016/S0040-4039(01)95462-0.
  10. ^ Griffin, B.E.; Jarman, M.; Reese, C.B. (1968). "The Synthesis of oligoribonucleotides—IV". Tetrahedron. 24 (2): 639–62. doi:10.1016/0040-4020(68)88015-9. PMID 5637486.
  11. ^ Ogilvie, Kelvin K.; Iwacha, Donald J. (1973). "Use of the tert-butyldimethylsilyl group for protecting the hydroxyl functions of nucleosides". Tetrahedron Letters. 14 (4): 317–9. doi:10.1016/S0040-4039(01)95650-3.
  12. ^ Paquette, Leo A.; Collado, Iván; Purdie, Mark (1998). "Total Synthesis of Spinosyn A. 2. Degradation Studies Involving the Pure Factor and Its Complete Reconstitution". Journal of the American Chemical Society. 120 (11): 2553–62. doi:10.1021/ja974010k. INIST:10388970.
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