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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17098생성일: 2026년 10월 25일

Formamide → 1-(3-Bromophenyl)ethanamine

https://huagongshe.com/reaction/17098

반응식

참여 물질

역할이름HCID투입량
반응물FormamideHCID 713—
반응물3'-BromoacetophenoneHCID 16502—
용매Formic AcidHCID 284—
생성물1-(3-Bromophenyl)ethanamineHCID 16785764—

반응 조건

온도220 °C

반응 단계

A mixture of commercially available 3-bromoacetophenone (30 g, 0.1508 mol), formic acid (47 mL) and formamide (70 mL) was heated to 220° C. for 5 h. The brown liquid obtained was cooled to RT, quenched with water and extracted with ethyl acetate. The organic layer was washed with water, brine and concentrated. The resulting brown liquid was dissolved in ethanol (375 mL) and conc. HCl (75 mL) and the mixture was refluxed over night. Ethanol was removed completely and the aqueous layer was washed with ether and ethyl acetate to remove all non-basic impurities. The aqueous layer was basified with a 10% aqueous sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, and concentrated to provide 26 g (86.65%) of A56.1. This compound was taken to the next step with out further purification. 1H NMR (CDCl3, 300 MHz) δ 1.38 (d, 3H), 4.1 (q, 1H), 7.2 (m, 1H), 7.27 (m, 1H), 7.37 (m, 1H), 7.51 (s, 1H). LS-MS (M−H)+=200.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737279B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e802393c4399432983187cfefc702fd7
출처 메모uspto-grants-2010_06