Reacción #2348112

ord-8600619d1cbd49889ca44dfe98058b03

Ecuación de reacción

CC(=O)OC1=CC(C)CCCCCCCCCCCC1
3-methylcyclopentadecene-1-yl acetate
CC1CCCCCCCCCCCCC(=O)C1
3-methylcyclopentadecanone
CC(=O)OC1=C[C@@H](C)CCCCCCCCCCCC1
(S)-3-methylcyclopenta-decenyl acetate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe hexane solution was purified by silica-gel column chromatography, and 3-methylcyclopentadecanone
  2. 2
    Otroas produced

Procedimiento

Mixed in 20 mL of a phosphate buffer (pH 7) were 2.0 g of dl-3-methylcyclopentadecene-1-yl acetate as obtained in Example 1 (a) and 1.0 g (50 wt. % relative to the substrate) of the immobilized enzyme (Novozyme 435) originating from Candida antarctica, followed by vigorous shaking at 55° C. for 2 days. After the reaction, 20 mL of hexane was added to the reaction solution for extraction, and analysis of the hexane layer showed that the conversion of the substrate was 69.8% and that 3-methylcyclopentadecanone was produced, while 3-methylcyclopentadecene-1-yl acetate remained. The hexane solution was purified by silica-gel column chromatography, and 3-methylcyclopentadecanone, as produced by hydrolyzing a portion of the remained 3-methylcyclopentadecene-1-yl acetate by the conventional method, was subjected to determination of the optical purity by HPLC and identified as the (S) isomer with 90.8% ee of optical purity. Also, 3-methylcyclopentadecanone, a enzymatic hydrolysate of the substrate, was subjected to determination of the optical purity and identified as the (R) isomer with 42.6% ee of optical purity.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07846701B2uspto-grants-2010_12