참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propanal | HCID 527 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Tert-butyl 1-oxo-8-azaspiro(4.5)decane-8-carboxylate | HCID 10848487 | — |
| 반응물 | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | tert-Butyl 2-(1-hydroxyprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate | HCID 21983945 | 120.9% |
반응 단계
tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate from Step G (4.5 g, 17.8 mmol) was dried by evaporating with toluene (10 mL) three times in vacuo, dissolved in tetrahydrofuran (100 mL), and cooled to −78° C. To this solution was added lithium diisopropylamide mono(tetrahydrofuran) (24 mL, 36 mmol, 1.5 M in cyclohexane). The reaction mixture was stirred for 30 min at −78° C. before adding propionaldehyde (2.6 mL, 36 mmol). After 5 min, the reaction mixture was diluted with diethyl ether, poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford 6.7 g of a clear oil. The residue was purified by flash chromatography eluting with 20–30% ethyl acetate in hexanes to give the title compound (4.75 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091211B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-f4d34c0f487347f9a801ff3387bd1e3d |
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| 출처 메모 | uspto-grants-2006_08 |
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