참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon tetrabromide | HCID 11205 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 1-Boc-2-Formylpyrrolidine | HCID 4227815 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-t-butyl 2-(2,2-dibromovinyl)pyrrolidine-1-carboxylate | HCID 14730281 | 86% |
반응 단계
A solution of triphenylphosphine (21.1 g, 80.3 mmol) and carbon tetrabromide (13.32 g, 40.16 mmol) in dichloromethane (300 mL) at 0° C. was treated with a solution of 2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (4.0 g, 20.08 mmol) in dichloromethane (10 mL) dropwise via syringe. The solution was stirred for 1 hour at room temperature, poured into a saturated sodium bicarbonate solution and separated. The organic phase was dried (MgSO4), filtered and concentrated. The concentrate was purified by flash chromatography on silica gel using 0–1% methanol/dichloromethane to give 6.13 g (86% yield) of the desired product. 1H NMR (300 MHz, CHLOROFORM-D) δ ppm 1.47 (s, 9H), 1.81 (m, 3H), 2.16 (m, 1H), 3.39 (m, 2H), 4.37 (s, 1H), 6.38 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07202363B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-7481ed778ec545a889a192434dd95c45 |
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| 출처 메모 | uspto-grants-2007_04 |
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