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HRID 2260929作成日:2026年10月26日

Hexane → Muskone

https://huagongshe.com/reaction/2260929

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物3-Methylcyclopentadecene-1-yl acetateHCID 68775372—
溶媒PhosphateHCID 1061—
生成物MuskoneHCID 10947—
生成物3-Methylcyclopentadecene-1-yl acetateHCID 68775372—

反応条件

温度55 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07846701B2
出典データセットuspto-grants-2010_12
ORD IDord-1371dba79beb42a09dabbd1cb50a9952
出典メモuspto-grants-2010_12