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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1062825생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1062825

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물Tert-butyl 6-cyano-5-hydroxy-3-oxohexanoateHCID 11637184—
용매TriglymeHCID 8189—
생성물1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoateHCID 22282997—

반응 조건

온도25 °C

반응 단계

Crude 5R 1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate (about 130 mmoles) from Step (1) is dissolved in the first distillate from the above Step (a) mixture and cooled to −75° C.±20° C. Sodium borohydride (6 g) as a solution in 75 mL triglyme is added slowly. After the addition, the reaction mixture is warmed to 25° C. The reaction mixture is quenched by the addition of 8 g acetic acid (and optionally 20 mL methanol) and concentrated by vacuum distillation—saving the distillate. The residue is dissolved in a mixture of water (100 mL) and ethyl acetate (200 mL), the layers separated, and the organic layer is concentrated by vacuum distillation. The residue is dissolved with 200 mL methanol and 10 mL acetic acid and concentrated by vacuum distillation. The residue is dissolved with 200 mL methanol and concentrated by vacuum distillation. The residue is dissolved with 200 mL methanol 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06962994B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-fc11ecaebe844ec6a6f6f4ee553274f2
출처 메모uspto-grants-2005_11