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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 451124생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/451124

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참여 물질

역할이름HCID투입량
반응물2-PhenylcyclohexanoneHCID 95592—
반응물Isocyanatocarbonyl chlorideHCID 119708—
용매Ethyl AcetateHCID 8857—
생성물8-phenyl-5,6,7,8-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dioneHCID 1051436819.62%
생성물4a-phenyl-4a,5,6,7-tetrahydro-2H-benzo[e][1,3]oxazine-2,4(3H)-dioneHCID 1053818235.3%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486952B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-ece7c552872f43cb8632bcaa31b47b50
출처 메모uspto-grants-2013_07