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HRID 259919作成日:2026年10月26日

Tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonate → Tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonate

https://huagongshe.com/reaction/259919

反応式

関与物質

役割名称HCID仕込み量
反応物Tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonateHCID 22917835—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonateHCID 9803422—

反応条件

温度25 °C

反応手順

0.2 g of 5% strength palladium on charcoal is added to a solution of 2.8 g of the laevorotatory isomer of tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonate in 50 cm3 of ethanol. The suspension is stirred for 2 hours at a temperature of about 25° C. under a hydrogen atmosphere (100 kPa). The catalyst is filtered off and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. 2.8 g of the laevorotatory isomer of tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonate are thus obtained in the form of an oil, used as such in the subsequent syntheses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05523469
出典データセットuspto-grants-1996_06
ORD IDord-e4772676ca694072bc9fb6329cecc7d7
出典メモuspto-grants-1996_06