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HRID 2090339作成日:2026年10月27日

Ammonia → 4-Bromo-alpha-methylbenzeneethanamine

https://huagongshe.com/reaction/2090339

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物1-(4-Bromophenyl)propan-2-oneHCID 736332—
反応物Sodium borohydrideHCID 4311764—
触媒Titanium isopropoxideHCID 11026—
溶媒EthanolHCID 702—
生成物4-Bromo-alpha-methylbenzeneethanamineHCID 205668—

反応手順

To a mixture of 2.0 M of ammonia in ethanol (117 mL, 235 mmol, Aldrich, Cat. No. 392685) and titanium tetraisopropoxide (27.7 mL, 93.9 mmol, Aldrich, Cat. No. 377996) was added 1-(4-bromophenyl)acetone (10.0 g, 46.9 mmol, Alfa Aesar, Cat. No. A19028). The reaction mixture was stirred at r.t. under nitrogen overnight. Sodium tetrahydroborate (2.66 g, 70.4 mmol) was added. The mixture was stirred at r.t. for additional 3 h. The reaction mixture was quenched with 2M ammonia in water, and filtered. The solid was washed with AcOEt. The filtrate was concentrated to remove most ethanol, and then was washed with AcOEt twice. The combined organic layers were extracted with 1N HCl aqueous solution (twice). The aqueous HCl solutions were combined, and adjusted with ammonia aqueous solution to pH=10. The result solution was extracted with CH2Cl2. The organic layer was dried with MgSO4, filtered, and concentrated to afford the desired compound which was directly used in the next step reaction without further purification. LCMS (M+H)+: m/z=214.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08436008B2
出典データセットuspto-grants-2013_05
ORD IDord-b1413a4f29a04d0095a49d9847b92f74
出典メモuspto-grants-2013_05