Isobutyric Acid → 2,2,4-Trimethyl-1-pentanol

HRID 477287

반응식

HRID 477287 반응식
[CH3:1][C:2]([CH3:10])([CH:5](O)[CH:6]([CH3:8])[CH3:7])[CH2:3][OH:4].C(O)(=O)C(C)C>>[CH3:1][C:2]([CH3:10])([CH2:5][CH:6]([CH3:8])[CH3:7])[CH2:3][OH:4]

참가 물질

3

실험 절차

Saturated trisubstituted alchols, such as 2,2,4-trimethyl-1-pentanol, have been produced for decades via several different proesses. In British Patent Specification 1,288,615, published Sept. 13, 1972 and issued to B. Yeomans, 2,2,4-trimethyl-1-pentanol is produced by a multi-step process that involves the esterification of 2,2,4-trimethylpentane-1,3-diol with isobutyric acid to produce 3-hydroxy-2,2,4-trimethylpentyl-1 isobutyrate, dehydration of the saturated hydroxyl ester to the unsaturated 2,2,4-trimethylpentenyl-1 isobutyrate, hydrogenation of the unsaturated ester to the saturated 2,2,4-trimethylpentyl-1 isobutyrate over a noble metal hydrogenation catalyst, and saponification of this saturated ester to 2,2,4-trimethyl-1-pentanol. In this reference the 2,2,4-trimethyl-1-pentanol is obtained by the saponification of the ester, not by a reduction process.

출처 및 근거

ORD 기록
ord-06a0a90b3d3d41039007f32e3e061fb5
출처 데이터셋
uspto-grants-1989_12
특허 번호
US04886919

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