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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290681Generated: November 3, 2026

Dimethylformamide → 2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehyde

https://huagongshe.com/reaction/1290681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
ReactantPhosphorus oxychlorideHCID 24813—
SolventTolueneHCID 1140—
Product2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehydeHCID 3448972—

Reaction Steps

Phosphorus oxychloride (92 g) was added dropwise to stirred DMF (78 ml) between 10°-15° C. To the resulting slurry was added 4-chlorophenylacetic acid (34.12 g). The resulting mixture was stirred at room temperature for one half hour and then heated to 70°-80° C. during 5.5 hours, during which time the mixture became effervescent. The reaction mixture was cooled and poured slowly onto cracked ice. The resulting suspension was brought to pH 10 with solid potassium carbonate. Ice was added intermittently during this addition to maintain the temperature below 15° C. Toluene (150 ml) was added and the resulting mixture heated at 100° C. for one hour. The mixture was cooled and allowed to stand overnight. The two resulting layers were separated and the aqueous layer extracted with toluene (2×100 ml). The combined organic layers were washed with water (5×200 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo and the resulting yellow solid was triturated with hexane to yield 26 g of 2-(4-chlorophenyl)-3-dimethylaminopropenal as a tan solid mp. 120°125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753642
Source datasetuspto-grants-1998_05
ORD IDord-2a4b4189cec343589f5175664d7aa798
Source noteuspto-grants-1998_05