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HRID 37119作成日:2026年10月25日
6-Oxabicyclo[3.1.0]hexane → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine
https://huagongshe.com/reaction/37119
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 6-Oxabicyclo[3.1.0]hexane | HCID 9244 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine | HCID 10535622 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine | HCID 19934564 | — |
反応手順
In 20 ml of N,N-dimethylformamide was dissolved 1.0 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine followed by addition of 0.24 g of sodium hydride. The mixture was stirred at 70° C. for 1 hour and after cooling to room temperature, 0.5 ml of cyclopentene oxide was added. The mixture was stirred at 70° C. for 3 hours. The reaction mixture was then allowed to cool, diluted with water and extracted with ethyl acetate. The extract was washed with water and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were recrystallized from ethyl acetate-hexane to give 0.53 g of 6-cyano-3,4-dihydro-4-(2-hydroxycyclopentan-1-yl)-2,2-dimethyl-2H-1,4-benzoxazine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05420126 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-658be5a07e2c441eb1bd87c04cd5b359 |
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| 出典メモ | uspto-grants-1995_05 |
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