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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 360031Generated: October 25, 2026

Acetic Acid → 1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoate

https://huagongshe.com/reaction/360031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethylmethoxyboraneHCID 522516—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoateHCID 22282997—

Reaction Conditions

Temperature-85 °C

Reaction Steps

Crude (R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3oxohexanoate, 21 g (0.0924 mol), is dissolved in 940 mL of tetrahydrofuran and 190 mL of methanol under a nitrogen atmosphere. This solution is cooled to -85° C. and 95 mL of a 15% solution of methoxydiethylborane in tetrahydrofuran is added. The reaction is cooled to -97° C. and 6.5 9 (0.172 mol) of sodium borohydride is added in 0.5 g portions over 1.5 hours. The reaction is maintained between -93° C. and -97° C. for 13 hours and allowed to warm to room temperature and stand for 60 hours under a nitrogen atmosphere. The reaction is quenched by the addition of 25 mL (0.395 mol) acetic acid and concentrated by vacuum distillation to an oil. The residue is dissolved with 500 mL methanol, concentrated by vacuum distillation, redissolved with 500 mL methanol and reconcentrated by vacuum distillation to give a dark brown oil. This oil is taken up in 500 mL of ethyl acetate and filtered through a plug of silica gel with the aid of 250 mL of ethyl acetate The solution is evaporated to give 15 g of crude [R-(R*,R*)]-1,1-dimethylethyl 6-cyano-3,5-dihydroxyhexanoate which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05003080
Source datasetuspto-grants-1991_03
ORD IDord-e90a17898c6a4640ab16726c4bb0569a
Source noteuspto-grants-1991_03