참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Benzaldehyde, 4-(2-hydroxyethoxy)- | HCID 89178 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(4-Formylphenoxy)ethyl methanesulfonate | HCID 22288650 | — |
반응 단계
Methanesulfonylchloride (3.3 mL) was added dropwise over 5 min to a solution of 4-(2-hydroxyethoxy)benzaldehyde (example 108, step a) (6.4 g) and triethylamine (6.4 mL) in DCM (30 mL) at 0° C. under argon. The resulting mixture was stirred at 0° C. for 10 min and then at RT for 1 h. The reaction mixture was washed with brine (2×30 mL), dried over sodium sulphate, filtered and evaporated in vacuo. The residue was purified by silica gel chromatography eluting with 40-50% EtOAc in petroleum ether (40-60° C.) to give the subtitled compound as a viscous yellow oil. Yield 8.87 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08148373B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-06a15d1e0f5d46a3847ad9b3d9ba2f12 |
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| 출처 메모 | uspto-grants-2012_04 |
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