関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl Chloride | HCID 7503 | — |
| 反応物 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 反応物 | Ethanamine, N,N-dimethyl-2-[2-[4-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]- | HCID 79514 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | Benzethonium Chloride | HCID 8478 | — |
反応手順
170.0 g of p-tert-octyl phenoxy ethoxy ethyl dimethylamine was added to a 1 L four-necked reaction flask, to which were sequentially added 100.2 g of methyl isobutyl ketone and 126.6 g of benzyl chloride. The reaction mixture was heated to reflux. The reaction was carried out for 2 hours. Then, 168.2 g of cyclohexane was added slowly. The flask was cooled to carry out crystallization. 156.8 g of a white solid was collected. The content of benzethonium chloride was 99.2% determined by titration according to the method described on page 247 of the United States Pharmacopeia USP29. The measured melting point was from 159.0 to 162.0° C. As calculated with reference to p-tert-octyl phenol, an overall yield of the three steps was less than 15%, which is remarkably far from that obtained by using a phase transfer catalyst. Thus, it does not have a practical application value.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09018418B2 |
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| 出典データセット | uspto-grants-2015_04 |
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| ORD ID | ord-69d54acfe72842e4a2738f575a5ce4ae |
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| 出典メモ | uspto-grants-2015_04 |
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