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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1062823생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1062823

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물Sodium borohydrideHCID 4311764—
반응물Tert-butyl 6-cyano-5-hydroxy-3-oxohexanoateHCID 11637184—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoateHCID 22282997—

반응 단계

Crude 5R 1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate (about 150 moles) from Step (1) is dissolved in the first distillate from Step (a) along with 50 L of tetrahydrofuran, cooled to −75° C.±20° C., and optionally diluted with 25 L of methanol, and 10 kg of acetic acid. Sodium borohydride (8 kg) as a solution in methanol and aqueous sodium hydroxide is added slowly. After the addition, the reaction mixture is warmed to 0° C.±25° C. The reaction mixture is quenched by the addition of 10 kg of acetic acid and 20 L of methanol and concentrated by vacuum distillation. The residue is dissolved in methanol and acetic acid, optionally diluted with water, and concentrated by vacuum distillation. The residue is dissolved in methanol and concentrated by vacuum distillation. The residue is dissolved in a mixture of water and ethyl acetate, and the aqueous layer separated. The organic layer is concentrated by vacuum distillation. The residue is dissolved in methanol and acetic acid and concentrated by vacuum distillation. The residue is dissolved in ethyl acetate and concentrated by vacuum distillation affording 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-ba9292c309024c0ebdb0fd1057be15e0
출처 메모uspto-grants-2005_11