Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730257Generated: October 30, 2026

Potassium Carbonate → 3-(4-tert-butylphenyl)-N-(3,4-dimethoxyphenyl)acrylamide

https://huagongshe.com/reaction/730257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-DimethoxyanilineHCID 22770—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(Tert-butyl)cinnamic acidHCID 724839—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-(4-tert-butylphenyl)-N-(3,4-dimethoxyphenyl)acrylamideHCID 10149955—

Reaction Steps

To a 20 mL round-bottomed flask equipped with reflux condenser and drying tube was added 4-tert-butyl-trans-cinnamic acid (200 mg, 0.98 mmol, EMKA-Chemie) followed by CH2Cl2 (5 mL), oxalyl chloride (90 uL, 130 mg, 1.03 mmol, Aldrich) and DMF (1 uL). The reaction mixture was magnetically stirred and heated at reflux for 30 min. The reaction mixture was concentrated in vacuo and the residue dissolved in acetone (2 mL). The solution was added to a mixture of 3,4-dimethoxyaniline (180 mg, 1.17 mmol, Aldrich), potassium carbonate (200 mg), water (2 mL) and acetone (2 mL), magnetically stirred at 25° C. in a 10 mL glass vial. The reaction mixture was stirred at 25° C. for 16 h then diluted with EtOAc (60 mL) and washed successively with 1 N HCl (20 mL), 1 N NaOH (20 mL), water (20 mL) and satd NaCl (20 mL), dried over MgSO4, filtered and concentrated. Recrystallization from hexane and CH2Cl2 provided the title product as a yellow solid. MP 115-116° C. MS (ESI, pos. ion) m/z: 340 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582657B2
Source datasetuspto-grants-2009_09
ORD IDord-c9da0f1e7c22481a994f11a0ad9ba582
Source noteuspto-grants-2009_09