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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11901생성일: 2026년 10월 24일

Hydrogen Bromide → 2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide

https://huagongshe.com/ko/reaction/11901

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanolHCID 9997789—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매IsopropanolHCID 3776—
생성물2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromideHCID 2197709680%

반응 단계

1.0 g of 2-(3-chloro-4-amino-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol was dissolved in 20 ml of anhydrous diethyl ether and the solution was acidified to pH=2 by adding dropwise a solution of hydrobromic acid in isopropanol with stirring. The precipitate was collected by filtration, washed with small amount of anhydrous diethyl ether, dried to give crude 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide. The crude product was dissolved in absolute ethanol at a ratio of 1:5 w/v. Filtered and anhydrous diethyl ether was added dropwise until small amount of crystals was precipitated. Lyophilized and filtered to give 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromide. Yield 80–90%; melting point 208–210° C. (dec). 1H-NMR (DMSO-d6) δ: 1.24(9H, s), 3.79(2H, d), 4.46–4.51(1H, m), 7.72(1H, s), 7.89(1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098364B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-484020b3048d494b90cf506b9fcdd076
출처 메모uspto-grants-2006_08