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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304039Generated: October 29, 2026

Sodium borohydride → 1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoate

https://huagongshe.com/reaction/2304039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl 6-cyano-5-hydroxy-3-oxohexanoateHCID 11637184—
SolventTriglymeHCID 8189—
Product1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoateHCID 22282997—

Reaction Steps

Crude 5R 1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate (about 150 mmoles) is dissolved in the first distillate from the above mixture, allowed to stir at room temperature for about 2 hours, and cooled to about −70° C. Sodium borohydride (6 g) as a solution in 75 mL triglyme is added slowly at between −65° C. to −75° C. After the addition, the reaction mixture is warmed to 15° C. to 25° C., quenched by the addition of acetic acid and concentrated by vacuum distillation. The residue is diluted with methanol and concentrated by vacuum distillation. The residue is dissolved in a mixture of water and ethyl acetate, the layers separated, and the organic layer is concentrated by vacuum distillation. The residue is dissolved with methanol and acetic acid and concentrated by vacuum distillation. The residue is dissolved in ethyl acetate and concentrated by vacuum distillation resulting in crude [R(R*,R*)]-1,1-dimethylethyl 6-cyano-3,5-dihydroxyhexanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433213B1
Source datasetuspto-grants-2002_08
ORD IDord-695b858ca63d4342b2509d54c40668a5
Source noteuspto-grants-2002_08