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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1774생성일: 2026년 10월 24일

2-Aminobenzophenone → 2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenone

https://huagongshe.com/ko/reaction/1774

반응식

참여 물질

역할이름HCID투입량
반응물2-AminobenzophenoneHCID 76080—
반응물Sodium BicarbonateHCID 516892—
용매Ethyl AcetateHCID 8857—
생성물2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenoneHCID 53932370—

반응 단계

A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726306
출처 데이터셋uspto-grants-1998_03
ORD IDord-947d3e4afae94a0b8dd4f97535b58d90
출처 메모uspto-grants-1998_03