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HRID 231839作成日:2026年10月24日

Benzyl Bromide → 1-benzyl-2-trifluoromethyl-(1H)-indole

https://huagongshe.com/ja/reaction/231839

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物2-(trifluoromethyl)-1H-indoleHCID 10932124—
反応物Monosodium phosphateHCID 23672064—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-benzyl-2-trifluoromethyl-(1H)-indoleHCID 17882580—

反応条件

温度0 °C

反応手順

8.6 g of 2-trifluoromethyl-(1H)-indole and 100 ml of tetrahydrofuran were mixed together under an inert atmosphere and cooled to 0° C. Over 15 minutes, about 2.4 g of a suspension of sodium hydride at 50% in oil was added in small fractions and 6.5 ml of benzyl bromide in solution in 10 ml of tetrahydrofuran were introduced over 5 minutes. The mixture was stirred for 42 hours at ambient temperature and then was poured into water saturated with monosodium phosphate. The mixture was extracted with ethyl ether, and the extracts were dried and concentrated to dryness by distillation under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of hexane and ethyl acetate (9/1) to obtain 12.54 g of 1-benzyl-2-trifluoromethyl-(1H)-indole melting at approx. 20° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04849443
出典データセットuspto-grants-1989_07
ORD IDord-6aba9620a94d47ac8f394f06fb33675d
出典メモuspto-grants-1989_07