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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44615생성일: 2026년 10월 23일

Ethyl benzoylformate → 1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dione

https://huagongshe.com/ko/reaction/44615

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl benzoylformateHCID 15349—
반응물Sodium hydrideHCID 24758—
반응물2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-oneHCID 57444113—
용매TetrahydrofuranHCID 8028—
생성물1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dioneHCID 5744411468%

반응 단계

To a solution of 0.22 g (0.81 mmol) of 2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-one in 5 mL of dry tetrahydrofuran cooled to −50° C., 0.10 g of sodium hydride 60% in mineral oil were added. The resulting suspension was maintained at the same temperature for 30 minutes and then 0.59 mL of ethyl α-oxobenzeneacetate (PhCOCOOEt) were added and the reaction mixture allowed to come to room temperature. After 16 hours the mixture was partitioned between water and ethyl acetate and the organic layer was dried over Na2SO4 and evaporated to dryness. The residue was purified by chromatography on a silica gel column (eluant hexane/ethyl acetate 7/3) giving 0.22 g (68% yield) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541429B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-6cb9fd63185241d28ffc6683e788d26e
출처 메모uspto-grants-2013_09