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HRID 2117271作成日:2026年10月25日

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

https://huagongshe.com/reaction/2117271

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PyridineHCID 1049—
反応物Methyl chloroformateHCID 6586—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物1,4-Dihydro-2H-3,1-benzoxazin-2-oneHCID 25786—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07442696B2
出典データセットuspto-grants-2008_10
ORD IDord-05284cd303c84f20bcc0d922ed50b7be
出典メモuspto-grants-2008_10