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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665971Generated: October 31, 2026

Dimethylformamide → 4-Bromo-3,5-dimethylbenzaldehyde

https://huagongshe.com/reaction/1665971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactantp-DibromoxyleneHCID 66875587—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product4-Bromo-3,5-dimethylbenzaldehydeHCID 22259686—

Reaction Steps

A solution of 2,5-dibromoxylene (8.0 g, 30.3 mmol) in diethyl ether (120 mL) is cooled to −78° C. and then treated with n-buthyllithium (20 mL, 1.6 M in hexane). After stirring for 40 min, DMF (6 mL) is slowly added. The mixture is warmed to it and stirred for 1 h. The mixture is cooled again to −78° C. before another portion of n-butyllithium (5 mL) is added. The reaction mixture is allowed to warm to it and stirred for another hour. The reaction is quenched by adding 5% aq. HCl. The mixture is extracted with EA, and the extract is concentrated in vacuo. The crude product is purified by CC on silica gel eluting with heptane:EA 5:1 to give 4-bromo-3,5-dimethyl-benzaldehyde (8.2 g) as a white soft solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039644B2
Source datasetuspto-grants-2011_10
ORD IDord-716e3b93141c46e480c72be35348eab4
Source noteuspto-grants-2011_10