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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695869Generated: October 31, 2026

Bromine → 5-Bromo-2-isopropylbenzaldehyde

https://huagongshe.com/reaction/1695869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Propan-2-yl)benzaldehydeHCID 590536—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-isopropylbenzaldehydeHCID 5834083534.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-isopropyl benzaldehyde (1.5 g, 10.13 mmole) in DCM (10 mL) was added to a solution of AlCl3 (2.6 g, 20.26 mmole) in DCM (10 mL) at 0° C. followed by addition of a dilute solution of Br2 (0.67 mL, 13.1 mmole in 20 mL DCM) to the reaction mixture. The solution was stirred at 0° C. for 6 hours then stirred overnight at room temperature. The reaction mixture was basified using saturated aqueous sodium bicarbonate and extracted with DCM (30×2 mL). The organic layers were combined and the crude product was obtained by evaporation of the solvent. The crude product was purified by column chromatography using 1% EtOAc in Hexane to yield 5-bromo-2-isopropylbenzaldehyde (800 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163704B2
Source datasetuspto-grants-2012_04
ORD IDord-b232da22878c462186a58b5c03af1879
Source noteuspto-grants-2012_04