참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(t-Butyl-amino)-N-methoxy-N-methyl-propanamide | HCID 22063402 | — |
| 반응물 | HCID 178418507 | HCID 178418507 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-tert-Butyl-4-piperidone | HCID 73840 | 32% |
반응 단계
3-(t-Butyl-amino)-N-methoxy-N-methyl-propanamide (5 g, 26.6 mmol, 1.0 equiv) was dissolved in dry THF (50 mL) under Ar. The solution was cooled to −78° C. and a 1 M solution of vinylmagnesium bromide (66.5 mL, 66.5 mmol, 2.5 equiv) was added dropwise over a 20 min period. The reaction was then stirred at −78° C. for 30 min and at 0° C. for 30 min at which time the reaction solution was transferred via a double-ended cannula into ice-cold saturated sodium bicarbonate solution under Ar. The mixture was stirred for 10 min and the crude product was extracted 2×150 mL EtOAc. The organic extracts were combined and concentrated in vacuo to a red oil. Purification was done by flash chromatography on silica using 100% CH2Cl2 through 4, 8, and 16% MeOH in CH2Cl2. The product was isolated as an orange oil (1.3 g, 32%); MS, m/z 156=M+1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06756372B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-7043cc7594874b548026b0834e04132c |
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| 출처 메모 | uspto-grants-2004_06 |
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