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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395893Generated: October 30, 2026

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

https://huagongshe.com/reaction/2395893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiethylmethoxyboraneHCID 522516—
ReactantSodium borohydrideHCID 4311764—
Reactant(R)-6-cyano-5-hydroxy-3-oxo-N,N-diphenylhexanamideHCID 9818592—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product6-cyano-3,5-dihydroxy-N,N-diphenylhexanamideHCID 22415340—

Reaction Conditions

Temperature-20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489691
Source datasetuspto-grants-1996_02
ORD IDord-e71c781eb1304a4aa7170cf81b79f589
Source noteuspto-grants-1996_02