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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

反応式

関与物質

役割名称HCID仕込み量
反応物6-Oxabicyclo[3.1.0]hexaneHCID 9244—
反応物Sodium hydrideHCID 24758—
反応物6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazineHCID 10535622—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazineHCID 19934564—

反応条件

温度70 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420126
出典データセットuspto-grants-1995_05
ORD IDord-658be5a07e2c441eb1bd87c04cd5b359
出典メモuspto-grants-1995_05