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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonate | HCID 22917835 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonate | HCID 9803422 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05523469 |
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| 出典データセット | uspto-grants-1996_06 |
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| ORD ID | ord-e4772676ca694072bc9fb6329cecc7d7 |
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| 出典メモ | uspto-grants-1996_06 |
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