関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-(7-Methoxy-1-naphthyl)ethanol | HCID 13570065 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(7-Methoxynaphthalen-1-yl)ethyl methanesulfonate | HCID 19085990 | — |
反応手順
2-(7-Methoxy-1-naphthyl)ethanol (25 mmol) and triethylamine (30 mmol) are dissolved in 50 ml of dichloromethane and the reaction mixture is cooled to 0° C. using an ice bath. Mesyl chloride (30 mmol) is added dropwise and the reaction mixture is stirred at ambient temperature for 2 hours and then poured into 100 ml of water. The organic phase is washed with 1M hydrochloric acid solution and then with water, dried over magnesium sulphate and evaporated. The oil obtained is precipitated from a mixture of diethyl ether/petroleum ether (1/1). The title product is filtered off under suction and then recrystallised from to diisopropyl ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947852B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-3ed8828f72094897973923c2cbadfc7a |
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| 出典メモ | uspto-grants-2011_05 |
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