참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Tetrahydro-3-furanmethanol | HCID 139980 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methanesulfonate | HCID 85257 | — |
| 생성물 | Tetrahydro-3-furanmethanol | HCID 139980 | — |
반응 단계
Triethylamine (13.7 mL, 98 mmol) was added to a solution of tetrahydro-3-furanmethanol (10.0 g, 98 mmol) in methylene chloride (100 mL) at 0° C. followed by addition of methanesulfonyl chloride (12.3 g, 108 mmol) dropwise. The reaction mixture was stirred at 0° C. for 1 h and then allowed to warm to ambient temperature and stirred overnight. Aqueous hydrochloric acid (1N, 100 mL) was added and the two layers were separated. The organic layer was washed with 1N aqueous hydrochloric acid (100 mL×2), saturated aqueous sodium bicarbonate (100 mL×3), and brine (50 mL×1), respectively. The organic phase was dried over anhydrous sodium sulfate and concentrated to afford crude mesylate of tetrahydro-3-furanmethanol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434761B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-75b92de63ae14e078729bd2eb9210720 |
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| 출처 메모 | uspto-grants-2016_09 |
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