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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20065Erstellt: 23. Oktober 2026

Boron tribromide → 3-Bromo-4-fluorobenzyl Bromide

https://huagongshe.com/de/reaction/20065

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron tribromideHCID 25134—
Edukt3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-4-fluorobenzyl BromideHCID 12922710—

Reaktionsschritte

(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745484B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-bdee873a287547a4bb709c42021939a4
Quellennotizuspto-grants-2010_06