関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phenethylamine | HCID 1001 | — |
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 1-Octanol, 8-chloro- | HCID 90012 | — |
| 溶媒 | tert-Butyl methyl ether | HCID 15413 | — |
| 生成物 | 8-(N-Benzyl-N-methylamino)octan-1-ol | HCID 16662153 | 96% |
反応手順
From 8-Chlorooctan-1-ol: A 2-L flask was charged with benzylmethylamine (270 g, 2.23 mol), sodium carbonate (157 g, 1.48 mol), sodium iodide (11.1 g, 0.074 mol), 8-chlorooctanol (122 g, 0.74 mol) and acetonitrile (1000 mL) and the resulting suspension was stirred at 80° C. for 20–30 h. The reaction mixture was then concentrated to a volume of about 500 mL and water (600 mL) and tert-butyl methyl ether (1000 mL) were added. The MTBE layer was then separated and washed with water (500 mL). The MTBE solution was concentrated by distillation under vacuum to provide an oil and the oil was then further concentrated by distillation under high vacuum to remove excess benzylmethylamine. N-methyl-2-pyrrolidone (300 mL) was then added to the remaining oil and this solution concentrated by distillation under high vacuum to provide an oil. The oil was dissolved in MTBE (1000 mL) and the resulting solution was washed with water (2×500 mL), brine (500 mL), dried with sodium sulfate (100 g), filtered and concentrated by distillation to afford the title compound as an oil (178 g, 96% yield, >95% purity).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07183292B2 |
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| 出典データセット | uspto-grants-2007_02 |
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| ORD ID | ord-2396a5983d5a474c8730bd84baf2517b |
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| 出典メモ | uspto-grants-2007_02 |
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