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HRID 2374642作成日:2026年10月26日

Borane → Benzenemethanamine, N-ethyl-4-(trifluoromethoxy)-

https://huagongshe.com/reaction/2374642

反応式

関与物質

役割名称HCID仕込み量
反応物BoraneHCID 6331—
反応物N-{[4-(Trifluoromethoxy)phenyl]methyl}acetamideHCID 44542707—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Benzenemethanamine, N-ethyl-4-(trifluoromethoxy)-HCID 2011772021%

反応条件

温度-10 °C

反応手順

N-[4-(Trifluoromethoxy)benzyl]acetamide (10.4 g, 44.6 mmol) was dissolved in THF (100 mL) and cooled to −10° C. Borane (56 mL of a 2 M solution of the dimethylsulfide complex in diethyl ether) was added and the reaction mixture was stirred at −10° C. for 15 minuters and was then allowed to warm to room temperature. The reaction mixture was refluxed overnight and was then allowed to cool to room temperature. The reaction was quenched by careful addition of 10% HCl (30 mL) at 0° C. and the mixture was stirred at room temperature overnight and then concentrated in, vacuo. The residue was taken up in water (200 mL) and diethyl ether (200 mL) and the phases were separated. Concentration in vacuo of the diethyl ether phase afforded 1.9 g (21%) of the title compound as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07462644B2
出典データセットuspto-grants-2008_12
ORD IDord-1a2021ab17924aba91c7657899c5d881
出典メモuspto-grants-2008_12