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HRID 340659作成日:2026年10月26日

Dimethylformamide → 2-(4-Benzyloxy-3-methoxyphenyl)benzothiazole

https://huagongshe.com/reaction/340659

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-AminothiophenolHCID 8713—
反応物Thionyl ChlorideHCID 24386—
反応物4-(Benzyloxy)-3-methoxybenzoic acidHCID 226335—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Benzyloxy-3-methoxyphenyl)benzothiazoleHCID 66911330—

反応条件

温度50 °C

反応手順

In methylene chloride (10 ml) was suspended 2.0 g (7.7 mmol) of 4-benzyloxy-3-methoxy benzoic acid. To this suspension was added 0.05 g of DMF and 0.68 ml of thionyl chloride, followed by stirring at 50° C. for 2 hours. This reaction solution was introduced dropwise at 0° C. into a solution wherein 1.2 g (9.3 mmol) of 2-aminothiophenol had been dissolved in 10 ml of pyridine at room temperature. The mixture was further stirred overnight at room temperature, diluted with water, and subjected to ethyl acetate extraction (50 ml×2 times). The extracts were dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue thus obtained was dissolved in 30 ml of toluene. This toluene solution was heated to reflux overnight while water was distilled off. Toluene was removed from this solution by distillation under reduced pressure, and the residue was purified using a silica gel column (eluant:ethyl acetate/hexane=1/5). The solvent was distilled off under reduced pressure. Using the crystals thus obtained, the desired compound was recrystallized in an amount of 0.18 g from methylene chloride-hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895599B2
出典データセットuspto-grants-2014_11
ORD IDord-601a2c7cf5f540bf80d41a7047f198a8
出典メモuspto-grants-2014_11