참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 2-(7-Methoxy-1-naphthyl)ethanol | HCID 13570065 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(7-Methoxynaphthalen-1-yl)ethyl methanesulfonate | HCID 19085990 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07947852B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
|---|
| ORD ID | ord-3ed8828f72094897973923c2cbadfc7a |
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| 출처 메모 | uspto-grants-2011_05 |
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