関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 1,3-Dibromopropane | HCID 8001 | — |
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | 3-Bromo-6-methoxybenzene-1,2-diol | HCID 3705874 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin | HCID 23272337 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06514996B2 |
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| 出典データセット | uspto-grants-2003_02 |
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| ORD ID | ord-7d65154f56be44c5b485c0d02beb4c0a |
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| 出典メモ | uspto-grants-2003_02 |
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