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4,4-Diethoxybutylamine → N-(4,4-diethoxybutyl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4,4-Diethoxybutylamine | HCID 80672 | — |
| 反応物 | Benzene sulphochloride | HCID 22564087 | — |
| 生成物 | N-(4,4-diethoxybutyl)benzenesulfonamide | HCID 70270548 | 86% |
反応手順
42 g 4-amino butyraldehyde diethyl acetal and 88 g benzene sulfochloride are processed as explained in Preparation Example 1. The reaction mixture is not clear from the very beginning and vigorous stirring is therefore indispensable. Methylene chloride is used for the extraction of the sulfonamide acetal. Yield: 86% based on the amino acetal used. The product will crystallize when standing for an extended time at room temperature; melting point: 109°-111° C.; for further purification recrystallization from a 2:1 volume mixture of water and ethanol is possible.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05849842 |
| 出典データセット | uspto-grants-1998_12 |
| ORD ID | ord-d9f122c8b3c4405781cfe5069be61f84 |
| 出典メモ | uspto-grants-1998_12 |