関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 反応物 | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| 反応物 | 5-Bromoindoline | HCID 3411566 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 5-Bromo-1-(2-nitrophenyl)-2,3-dihydro-1H-indole | HCID 13823332 | 55% |
反応手順
5-Bromoindoline (4.0 g, 0.02 mole), collidine (3.6 g, 0.03 mole), and o-fluoronitrobenzene (2.8 g, 0.02 mole) in xylene (25 ml) were heated at 185° C. (oil bath temperature) for 24 hours. The mixture was cooled to room temperature and poured into dichloromethane. The dichloromethane solution was washed with 1N hydrochloric acid (3 times, 150 ml), brine (200 ml), dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated. Crystallization of the residue was induced by stirring in ether (15 ml) followed by hexane (200 ml), then chilling in the refrigerator overnight. The solid was filtered and washed with hexane and dried to yield 3.5 g (55%) of product. Recrystallization from 2-propanol yielded the analytical sample, mp 12°-114° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04723003 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-29f5254ffce34974b22ac7032000c5f7 |
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| 出典メモ | uspto-grants-1988_02 |
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