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HRID 1019319作成日:2026年10月27日
Stearamidopropyl Dimethylamine → N,N-dimethyl-N-(3-methyl-4-isopropylphenyl)oxycarbonylmethyl-N-(3-(octadecanoylamino)propyl)ammonium chloride
https://huagongshe.com/reaction/1019319
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Stearamidopropyl Dimethylamine | HCID 62109 | — |
| 反応物 | Chloroacetate | HCID 518964 | — |
| 反応物 | 3-Methyl-4-isopropylphenyl chloroacetate | HCID 12084261 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | N,N-dimethyl-N-(3-methyl-4-isopropylphenyl)oxycarbonylmethyl-N-(3-(octadecanoylamino)propyl)ammonium chloride | HCID 12084278 | 78% |
反応手順
A 33.18 g (0.090 mol) portion of N-octadecanoyl-N′,N′-dimethyl-1,3-diaminopropane and 120 ml of chloroform were put into a flask, and 22.44 g (0.099 mol) of 3-methyl-4-isopropylphenyl chloroacetate was added thereto at 25° C. spending 5 minutes. The reaction mixture was stirred at 25° C. for 36 hours and then, after confirming disappearance of the most part of chloroacetate by 1H-NMR, the solvent was evaporated under a reduced pressure. The thus obtained viscous oil was dissolved in 300 ml of acetone and cooled to 5 to 10° C. to effect precipitation of a white precipitate. Thereafter, in the same manner as described in Inventive Example 1, the title compound (to be referred to as betaine ester (12) hereinafter) was obtained as a white solid. Yield 41.80 g (0.070 mol; yield 78.0%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06486333B1 |
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| 出典データセット | uspto-grants-2002_11 |
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| ORD ID | ord-c919553694564978aba17363784f88b9 |
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| 出典メモ | uspto-grants-2002_11 |
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