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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018807Generated: October 31, 2026

Dimethylformamide → 3-Chloro-3-[3-chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]propenal

https://huagongshe.com/reaction/1018807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium ethoxideHCID 2723922—
Reactant1-[3-Chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanoneHCID 22390425—
SolventDichloromethaneHCID 6344—
Product3-Chloro-3-[3-chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]propenalHCID 57214517—

Reaction Steps

3.51 ml of oxalyl chloride are added dropwise at a temperature of between −5° C. and 2° C. to a solution of 3.72 ml of dimethylformamide and 20 ml of anhydrous dichloromethane and the reaction mixture is then stirred at room temperature for 30 minutes. 3.92 g of 1-[3-chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone (compound V.6) dissolved in 10 ml of dichloromethane are then added rapidly, after which the reaction mixture is stirred at room temperature for 12 hours. The reaction mixture is poured into a water/ice mixture and 20 ml of aqueous 2.84 M sodium ethoxide solution are then added. The resulting mixture is washed with 50 ml of sodium hydrogen carbonate solution and 50 ml of water, the phases are separated after settling has taken place, the organic phase is dried over magnesium sulphate and the solvents are evaporated off under reduced pressure. The oil obtained is purified by chromatography on a column of silica gel, eluting with a 97/3 (v/v) cyclohexane/ethyl acetate mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482986B1
Source datasetuspto-grants-2002_11
ORD IDord-f8dedd069e3949489c2edd6a2d370b42
Source noteuspto-grants-2002_11