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HRID 240543作成日:2026年10月27日

Boron tribromide → 2-Methyl-1,3-benzothiazol-6-ol

https://huagongshe.com/reaction/240543

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6-Methoxy-2-methylbenzothiazoleHCID 76254—
溶媒DichloromethaneHCID 6344—
生成物2-Methyl-1,3-benzothiazol-6-olHCID 75930444.3%

反応手順

To a cooled (−78° C.) solution of 6-methoxy-2-methylbenzo[d]thiazole (0.861 g, 4.80 mmol) in dichloromethane (10 mL) was added BBr3 (5 mL of 1.0 M solution in dichloromethane). After slowly warming to room temperature and stirring for 16 hours, the mixture was cooled to 0° C. and slowly quenched with methanol (20 mL). The reaction mixture was warmed to room temperature and concentrated under reduced pressure. The residue was partitioned between saturated NaHCO3 and dichloromethane/isopropyl alcohol (85/15). The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to provide the crude product (0.351 g, 44%) that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648087B2
出典データセットuspto-grants-2014_02
ORD IDord-33b628fc50b2431cbbc37ee7eb720c52
出典メモuspto-grants-2014_02