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HRID 488678作成日:2026年10月25日

Boron tribromide → 1,3-Benzenediol, 5-chloro-

https://huagongshe.com/reaction/488678

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1-Chloro-3,5-dimethoxybenzeneHCID 81502—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1,3-Benzenediol, 5-chloro-HCID 94554—

反応手順

A solution of 5-chloro-1,3-dimethoxybenzene (5.41 g, 31.3 mM) in methylene chloride (75 mL) at −78° C. was stirred with a 1M solution of BBr3 in methylene chloride (63 mL) for 45 minutes. The reaction was allowed to warm to room temperature overnight and diluted with water (75 mL). The layers were separated and the aqueous layer washed two times with methylene chloride. The aqueous layer was acidified with 1N HCl and extracted 3 times with ethyl acetate. The combined organic layers were washed with 1N sodium thiosulfate (1×35 mL) and water (1×25 mL). The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure and purified by chromatography (methylene chloride/acetone) to provide the titled compound. MS ESI(−)) m/e 143 (M−H)+; 1H NMR (300 MHz, CDCl3) δ 6.45 (d, 2H), 6.25 (t, 1H), 5.41 (bs, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06972340B2
出典データセットuspto-grants-2005_12
ORD IDord-d02b4d6792e54ef49b8f8bdf66bdb5ba
出典メモuspto-grants-2005_12