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HRID 413308作成日:2026年10月24日

Boron tribromide → 4-(1,2,3-Thiadiazol-4-Yl)Phenol

https://huagongshe.com/ja/reaction/413308

反応式

関与物質

役割名称HCID仕込み量
反応物Boron tribromideHCID 25134—
反応物4-(4-Methoxyphenyl)-1,2,3-thiadiazoleHCID 2739349—
溶媒DichloromethaneHCID 6344—
生成物4-(1,2,3-Thiadiazol-4-Yl)PhenolHCID 279686094.3%

反応条件

温度-78 °C

反応手順

4-(4-methoxy-phenyl)-[1,2,3]thiadiazole (1.06 g, 5.50 mmol) was dissolved in methylene chloride (20 ml) and the solution was cooled to about −78° C. Boron tribromide (1.0 M in methylene chloride, 12.1 ml) was added dropwise to the solution to afford a brown-colored solution. The reaction mixture was allowed to stir for about fifteen minutes, the cooling bath was removed, and the mixture was allowed to stir at room temperature for about an additional twelve hours. The mixture was poured into water, and the resulting mixture was adjusted to about pH 6. The mixture was extracted with methylene chloride (3×100 ml), and the combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 924 mg (94% yield) of the desired title compound as a tan solid. LRMS ([M+H]+)=179.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06566377B2
出典データセットuspto-grants-2003_05
ORD IDord-7a97b6e098e742eaa10e136297d75d58
出典メモuspto-grants-2003_05