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HRID 477598作成日:2026年10月26日

Water → 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone

https://huagongshe.com/reaction/477598

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl bromoacetateHCID 7748—
反応物Sodium hydrideHCID 24758—
反応物6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 13957955—
溶媒DimethylformamideHCID 6228—
生成物3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 1401424425%

反応条件

温度0 °C

反応手順

50% Oily sodium hydride (0.21 g) was suspended in N,N-dimethylformamide (5 ml), and the resultant suspension was cooled to 0° C. 6-Fluoro-5-nitro-2(3H)-benzothiazolone (1.0 g) was portionwise added thereto at 0° C., and the mixture was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (0.86 g) was added to the reaction mixture at 0° C., and the temperature was gradually elevated to a temperature of 50° to 60° C., followed by stirring at that temperature for 3 hours. Water was added to the mixture, which was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9) to give 0.35 g of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone, m.p., 139.0°-140.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04888428
出典データセットuspto-grants-1989_12
ORD IDord-33779e788a05417badbe4024f628ef3d
出典メモuspto-grants-1989_12