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HRID 20065作成日:2026年10月25日

Boron tribromide → 3-Bromo-4-fluorobenzyl Bromide

https://huagongshe.com/reaction/20065

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3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-4-fluorobenzyl BromideHCID 12922710—

反応手順

(3-Bromo-4-fluorophenyl)methanol (0.264 g, 1.29 mmol) was dissolved in DCM (3 mL). The solution was cooled to 0 deg, and tribromoborane (1.0 M in DCM, 0.863 ml, 0.863 mmol) was added. The mixture was stirred at 0 deg for 1 h, then rt for 1 h. The reaction was quenched with water, and the mixture was transferred to a separatory funnel with half-saturated NaHCO3 (15 mL), and the aqueous phase was extracted with DCM (3×20 mL). The organics were combined, washed with half-saturated brine (5 mL), dried over sodium sulfate and concentrated. Purification of the residue through silica gel (40 mL) using 5% EtOAc-hexane afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745484B2
出典データセットuspto-grants-2010_06
ORD IDord-bdee873a287547a4bb709c42021939a4
出典メモuspto-grants-2010_06