참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1,3-Dibromopropane | HCID 8001 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 3-Bromo-6-methoxybenzene-1,2-diol | HCID 3705874 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin | HCID 23272337 | — |
반응 단계
3-bromo-6-methoxycatechol (31 g) was dissolved in DMF (50 ml), mixed with 1,3-dibromopropane (36 ml) and potassium fluoride (42 g), stirred for 12 hours while heating at 110° C. The resultant was allowed to stand for cooling, mixed with water, and extracted with ether. The organic layer was washed with an aqueous sodium hydroxide solution, water, and a saturated aqueous sodium chloride solution in that order, dried over manganese sulfate, and evaporated under reduced pressure for removing the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give Compound IIbr-a (6.7 g, 18%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06514996B2 |
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| 출처 데이터셋 | uspto-grants-2003_02 |
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| ORD ID | ord-7d65154f56be44c5b485c0d02beb4c0a |
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| 출처 메모 | uspto-grants-2003_02 |
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