Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075014Generated: October 30, 2026

Carbon tetrabromide → 1-Bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2075014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Bromo-5-(trifluoromethyl)benzyl alcoholHCID 2756248—
SolventDichloromethaneHCID 6344—
Product1-Bromo-2-(bromomethyl)-4-(trifluoromethyl)benzeneHCID 275624970.1%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of (2-bromo-5-(trifluoromethyl)phenyl)methanol (4.7 g, 18 mmol) in methylene chloride (50 mL) at −10° C. was added carbon tetrabromide (CBr4) (7.17 g, 21.6 mmol). The resulting mixture was stirred at −10° C. for 15 minutes. Triphenylphosphine (5.61 g, 21.4 mmol) was then slowly added portionwise. This mixture was stirred at room temperature for 16 hours. The mixture was partitioned between saturated ammonium chloride (NH4Cl) (50 ml) and methylene chloride (2×50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4) and concentrated. The residue was purified by flash chromatography (silica gel) (eluted with 3:1 hexanes-ethyl acetate) to yield the title compound as a white solid (4.01 g). 1H NMR (400 MHz, CDCl3) δ 4.6 (s, 2H) 7.5 (dd, J=8.3, 1.6 Hz, 1H) 7.8 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919506B2
Source datasetuspto-grants-2011_04
ORD IDord-301daa5019ac463bb51218ea12bbb7ec
Source noteuspto-grants-2011_04