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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389696Generated: October 30, 2026

Bromine → 5-Bromo-2-ethylbenzaldehyde

https://huagongshe.com/reaction/2389696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2-EthylbenzaldehydeHCID 123406—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-ethylbenzaldehydeHCID 54772389—

Reaction Steps

A stirred suspension of 2-ethylbenzaldehyde (0.98 mL, 7.45 mmol) and AlCl3 (1.74 g, 13 mmol) in DCM (4.5 mL) at 0° C. is treated with a solution of Br2 (0.38 mL, 7.45 mmol) in DCM (4.5 mL) dropwise over 6 h then stirred 16 h at RT. After this time, the reaction mixture is poured over ice-water (50 mL), the layers separated and the aqueous layer extracted with DCM (3×50 mL). The organic phases are combined and washed with 2M HCl (100 mL), aqueous NaHCO3 (100 mL) and brine (100 mL), dried over Na2SO4 then the solvents removed in vacuo. Purification by column chromatography (gradient elution—100% heptane increasing to 10% EtOAc in heptane) gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273747B2
Source datasetuspto-grants-2012_09
ORD IDord-3997b46c88c94175bff54c21c88b77de
Source noteuspto-grants-2012_09