참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Veratryl alcohol | HCID 7118 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-Bromo-3,5-difluorobenzene | HCID 136313 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-Bromo-3-(3,4-dimethoxybenzyloxy)-5-fluorobenzene | HCID 19426985 | 83% |
반응 단계
Sodium hydride (80% disp. in oil; 933 mg, 31.1 mmol) was added, all at once, to 3,4-dimethoxybenzyl alcohol (3.48 g, 20.7 mmol) in DMF (40 mL) at 0° C. and under Ar. After 5 min., the mixture was allowed to warm to r.t. After 1 h, 1-bromo-3,5-difluorobenzene (4 g, 20.7 mmol) in DMF (5 mL) was added dropwise at r.t. The resulting mixture was kept at this temperature for 16 h and slowly poured into H2O (500 mL). It was extracted with EtOAc (3×) and the combined organics were washed with 25% NH4OAc buffer (1×), H2O (2×) and brine. The solution was dried (MgSO4) and concentrated to give a pale yellow solid that was purified by column chromatography on silica gel (EtOAc:hexane, 10:90-15:85) to afford the title compound as a white solid (5.85 g, 83%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05552437 |
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| 출처 데이터셋 | uspto-grants-1996_09 |
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| ORD ID | ord-c889a227ae3b411caa138f2b695a4ed7 |
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| 출처 메모 | uspto-grants-1996_09 |
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