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HRID 2117271생성일: 2026년 10월 24일

Water → 1,4-Dihydro-2H-3,1-benzoxazin-2-one

https://huagongshe.com/ko/reaction/2117271

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물Methyl chloroformateHCID 6586—
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물1,4-Dihydro-2H-3,1-benzoxazin-2-oneHCID 25786—

반응 단계

Methyl chloroformate (1.2 equiv) is added to a solution of a 2-(aminophenyl)alkanol (1 equiv) and DMAP (0.10 equiv) in pyridine (1 M) at 0° C. Additional pyridine is added as needed to keep the precipitates from accumulating. The solution is allowed to warm to room temperature and stirred for 2 hours. Sodium bisulfate (2N) and ethyl acetate are added, resulting in an aqueous layer and a first organic layer. The first organic layer is collected and the aqueous layer extracted with ethyl acetate. The organic layer from that extraction is combined with the first organic layer and that combined organic layer is washed sequentially with water and brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to afford a solid. To the solid is added potassium carbonate (2 equiv) in DMF (0.5-0.7 M) and that mixture is heated to 100° C. for 1-4 hours. The mixture is cooled and poured into ethyl acetate:water, resulting in a first organic layer and an aqueous layer. The first organic layer is collected and the aqueous layer is extracted with ethyl acetate. The organic layer from that extraction is combined with the collected first organic layer, and the combined organic layers are washed sequentially with water and brine, dried over magnesium sulfate, filtered, and concentrated to afford the 1,4-dihydro-2H-3,1-benzoxazin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07442696B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-05284cd303c84f20bcc0d922ed50b7be
출처 메모uspto-grants-2008_10