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HRID 451124作成日:2026年10月25日

2-Phenylcyclohexanone → 4a-phenyl-4a,5,6,7-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dione

https://huagongshe.com/reaction/451124

反応式

関与物質

役割名称HCID仕込み量
反応物2-PhenylcyclohexanoneHCID 95592—
反応物Isocyanatocarbonyl chlorideHCID 119708—
溶媒Ethyl AcetateHCID 8857—
生成物8-phenyl-5,6,7,8-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dioneHCID 1051436819.62%
生成物4a-phenyl-4a,5,6,7-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dioneHCID 1053818235.3%

反応条件

温度130 °C

反応手順

A solution of 2-phenylcyclohexanone (1.500 g, 8.61 mmol) and carbonisocyanatidic chloride (0.966 mL, 12 mmol) was stirred at 58° C. in a high-pressure vessel (75 mL) for 1 h. The temperature was raised to 130° C. and the reaction mixture was stirred for 2 h. After cooling to room temperature, the reaction mixture solidified. The solid residue was dissolved in ethyl acetate and washed with saturated aqueous solution of sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate and filtered. The solvent was removed in vacuum and the oily residue was purified by column chromatography on silica gel to provide 8-phenyl-5,6,7,8-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dione (415.0 mg, 1.689 mmol, 19.62% yield) as white solid and 4a-phenyl-4a,5,6,7-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dione (746.4 mg, 3.04 mmol, 35.3% yield) as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486952B2
出典データセットuspto-grants-2013_07
ORD IDord-ece7c552872f43cb8632bcaa31b47b50
出典メモuspto-grants-2013_07