참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | (R)-4-bromo-alpha-methylbenzylamine | HCID 853000 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[(1R)-1-(4-bromophenyl)ethyl]acetamide | HCID 793485 | 100% |
반응 단계
To a stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.52 g, 2.59 mmol) in anhydrous CH2Cl2 (5 mL) under argon were added acetic anhydride (0.37 mL, 3.89 mmol) and Pyridine (0.31 mL, 3.89 mmol). The resulting solution was stirred at 25° C. for 3 hrs. The reaction mixture was quenched with saturated 1N HCl and extracted with EtOAc (30 mL). The organic phase was washed with brine (50 mL), dried over Na2SO4 and evaporated. The residue was purified by flash column chromatography (80% EtOAc in hexanes) to give the product (0.62 g, 100%) as a white solid. 1H NMR (CDCl3) δ: 1.46 (d, J=7.0 Hz, 3H), 1.99 (s, 3H), 5.03-5.12 (m, 1H), 5.68 (brs, 1H), 7.18 (d, J=8.4 Hz, 2H), 7.47 (d, J=8.4 Hz, 2H). ESIMS (MNa+): 264.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07473790B2 |
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| 출처 데이터셋 | uspto-grants-2009_01 |
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| ORD ID | ord-aff036d6eba140e79129cd39e1aa9468 |
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| 출처 메모 | uspto-grants-2009_01 |
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