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HRID 11901作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanolHCID 9997789—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒IsopropanolHCID 3776—
生成物2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylamino-ethanol hydrobromideHCID 2197709680%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098364B2
出典データセットuspto-grants-2006_08
ORD IDord-484020b3048d494b90cf506b9fcdd076
出典メモuspto-grants-2006_08