Reacción #564469

ord-06a0a90b3d3d41039007f32e3e061fb5

Ecuación de reacción

CC(C)C(O)C(C)(C)CO
2,2,4-trimethylpentane-1,3-diol
CC(C)C(=O)O
isobutyric acid
CC(C)CC(C)(C)CO
2,2,4-trimethyl-1-pentanol

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04886919uspto-grants-1989_12