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HRID 964948생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/964948

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium HydroxideHCID 14797—
반응물3-ChloropropiophenoneHCID 70295—
반응물1H-2,3-Benzothiazin-4(3H)-one 2,2-dioxideHCID 89042—
용매MethanolHCID 887—
생성물3-(3-Oxo-3-phenylpropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-DioxideHCID 1907442368%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773437
출처 데이터셋uspto-grants-1998_06
ORD IDord-4ded7243862b45d28d9890b39ac01a35
출처 메모uspto-grants-1998_06