참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | Tert-butyl 6-cyano-5-hydroxy-3-oxohexanoate | HCID 11637184 | — |
| 용매 | Triglyme | HCID 8189 | — |
| 생성물 | 1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoate | HCID 22282997 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06962994B2 |
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| 출처 데이터셋 | uspto-grants-2005_11 |
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| ORD ID | ord-fc11ecaebe844ec6a6f6f4ee553274f2 |
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| 출처 메모 | uspto-grants-2005_11 |
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