돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1453022생성일: 2026년 10월 26일

Pyridine → N-[(1R)-1-(4-bromophenyl)ethyl]acetamide

https://huagongshe.com/reaction/1453022

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetic AnhydrideHCID 7918—
반응물(R)-4-bromo-alpha-methylbenzylamineHCID 853000—
용매DichloromethaneHCID 6344—
생성물N-[(1R)-1-(4-bromophenyl)ethyl]acetamideHCID 793485100%

반응 조건

온도25 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07473790B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-aff036d6eba140e79129cd39e1aa9468
출처 메모uspto-grants-2009_01