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HRID 129941作成日:2026年10月27日

Methanol → 6-cyano-3,5-dihydroxy-N,N-diphenylhexanamide

https://huagongshe.com/reaction/129941

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物DiethylmethoxyboraneHCID 522516—
反応物Sodium borohydrideHCID 4311764—
反応物(R)-6-cyano-5-hydroxy-3-oxo-N,N-diphenylhexanamideHCID 9818592—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物6-cyano-3,5-dihydroxy-N,N-diphenylhexanamideHCID 22415340—

反応条件

温度-20 °C

反応手順

Crude (R)-6-cyano-5-hydroxy-3-oxo-N,N-diphenylhexanamide, approximately 0.2 mol, is dissolved in tetrahydrofuran (200 mL) and methanol (100 mL) under a nitrogen atmosphere. The solution is cooled to -20° C., and a 50% solution of methoxydiethylborane in tetrahydrofuran (105 mL) is added. The reaction is cooled to -78° C., and sodium borohydride (24 g, 0.63 mol) is added over 30 minutes. The reaction mixture is maintained at -78° C. for 5 hours, allowed to warm to room temperature, and stand for 10 hours under a nitrogen atmosphere. The reaction is quenched by the addition of acetic acid (40 mL) and concentrated by vacuum distillation to an oil. The residue is dissolved with methanol (400 mL), concentrated by vacuum distillation, redissolved with methanol (300 mL), and reconcentrated by vacuum distillation to give a yellow oil. The oil is taken up in ethyl acetate (300 mL) and washed with deionized water (500 mL). The ethyl acetate solution is concentrated by vacuum distillation to give [R-(R*,R*)])-6-cyano-3,5-dihydroxy-N,N-diphenylhexanamide as an oil which is used without further purification. A small sample is purified by column chromatography on flash silica gel (60:40 hexane:ethyl acetate) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470981
出典データセットuspto-grants-1995_11
ORD IDord-e4541bd1e5c44a11a5b38bf72aa238f9
出典メモuspto-grants-1995_11