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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19778Generated: October 26, 2026

Hydrochloric Acid → 4-Chloro-3-ethylbenzaldehyde

https://huagongshe.com/reaction/19778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant4-Bromo-1-chloro-2-ethylbenzeneHCID 44119401—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product4-Chloro-3-ethylbenzaldehydeHCID 5526509562.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4.319 g of 4-bromo-1-chloro-2-ethyl-benzene (20 mmol) in 50 ml diethylether, cooled to 0° C., were added dropwise 12.3 ml of 1.6M n-BuLi in hexane. After 30 min. stirring at 0° C. and 2 h at RT, a solution of 2.43 ml DMF (31 mmol) in 10 ml diethylether was added dropwise (temperature raised from 20 to 28° C.). After 1 h additional stirring at RT, the reaction mixture was acidified with 2N HCl, diluted with 150 ml water and extracted with diethylether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by flash column chromatography (heptane/AcOEt: 95/5) to yield 2.1 g of a colorless oil. MS (ISP) 168.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745477B2
Source datasetuspto-grants-2010_06
ORD IDord-71d96795f3b74acda950d9f94cb7eed1
Source noteuspto-grants-2010_06