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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643576Generated: October 31, 2026

Benzyl Bromide → Benzyl 4-bromo-2-fluorobenzoate

https://huagongshe.com/reaction/1643576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant4-Bromo-2-fluorobenzoic acidHCID 302681—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-bromo-2-fluorobenzoateHCID 22351348102.4%

Reaction Steps

Benzyl bromide (2.80 mL, 23.6 mmol) was added to a solution of 2-fluro-4-bromobenzoic acid (4.34 g, 19.8 mmol) and Cs2CO3 (9.79 g, 30.0 mmol) in CH2Cl2 (50 mL). The mixture was heated to reflux for 4 hr. The reaction was quenched with H2O (150 mL) and extracted with CH2Cl2 (150 mL). The organic layer was dried over MgSO4 and concentrated. The residue was purified by flash column chromatograph eluting with 10% EtOAc in hexanes to give a colorless oil (6.27 g, 100% yield). 1H NMR (400 MHz, CDCl3) δ 7.82-7.88 (m, 1 H) 7.44-7.47 (m, 2 H) 7.34-7.42 (m, 5 H) 5.38 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-b7afaf51ac4b46d5b7ebc9b55ed5abf4
Source noteuspto-grants-2012_02