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HRID 964948作成日:2026年10月26日

Dimethylformamide → 3-(3-Oxo-3-phenylpropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-Dioxide

https://huagongshe.com/reaction/964948

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium HydroxideHCID 14797—
反応物3-ChloropropiophenoneHCID 70295—
反応物1H-2,3-Benzothiazin-4(3H)-one 2,2-dioxideHCID 89042—
溶媒MethanolHCID 887—
生成物3-(3-Oxo-3-phenylpropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-DioxideHCID 1907442368%

反応手順

1H-2,3-Benzothiazin-4(3H)-one 2,2-dioxide (1 g, 5.08 mmol.) was added to a solution of powdery potassium hydroxide (334 mg, 5.08 mmol.) in methanol (4 mL). The mixture was then stirred at room temperature for 15 min. The solution was placed under reduced pressure to distill the solvent off to dryness. To the dried product were added 3-chloropropiophenone (856 mg, 5.08 mmol.) and dimethylformamide (8 mL). The mixture was heated to 120° C. for 6 hours under stirring. The reaction liquid was placed under reduced pressure to distill the solvent off. To the resulting residue was added water, and it was extracted with ethyl acetate. The extract solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The dried extract solution was placed under reduced pressure to distill the solvent off. The resulting oil was treated by silica gel column chromatography (chloroform) to give the desired compound (1.13 g, yield 68%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05773437
出典データセットuspto-grants-1998_06
ORD IDord-4ded7243862b45d28d9890b39ac01a35
出典メモuspto-grants-1998_06