参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 叔丁醇 | HCID 6386 | — |
| 反应物 | Hydride | HCID 166653 | — |
| 反应物 | 3-叔丁基环丁酮 | HCID 10931442 | — |
| 反应物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶剂 | 四氢呋喃 | HCID 8028 | — |
| 产物 | HCID 178445820 | HCID 178445820 | — |
反应步骤
Cool lithium aluminum hydride (16 mL, 16 mmol, 1.0 M solution in tetrahydrofuran) under a nitrogen atmosphere to 0° C. Add tert-butanol (4.6 mL, 48.1 mmol) dropwise, warm to room temperature, and stir the resulting solution for 1 hour. Cool the hydride solution to −78° C. and add a solution of 3-tert-butylcyclobutanone (1 g, 7.9 mmol) in dry tetrahydrofuran (3 mL) dropwise. Stir for 1 hour at −78° C. and then warm to room temperature over 1 hour. Slowly quench the mixture with 0.1 N hydrochloric acid. Dilute the resulting mixture with ethyl acetate and a saturated aqueous solution of sodium potassium tartrate (Rochelle salt) and stir the biphasic mixture overnight. Filter the mixture to remove precipitates and separate the aqueous layer. Saturate the aqueous phase with sodium chloride and extract with ethyl acetate. Add the organic extract to the ethyl acetate solution of the reaction mixture and wash the resultant mixture with saturated aqueous sodium chloride solution, dry (magnesium sulfate), filter, and concentrate to give the title compound as a 9:1 mixture of cis/trans diastereomers.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07745438B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-2df14d6ee4694d99b4c524f669c21778 |
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| 来源说明 | uspto-grants-2010_06 |
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