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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730256Generated: October 29, 2026

Aniline → (E)-3-(4-tert-Butyl-phenyl)-N-phenyl-acrylamide

https://huagongshe.com/reaction/730256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDichloromethaneHCID 6344—
Reactant4-(Tert-butyl)cinnamic acidHCID 724839—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventEthyl AcetateHCID 8857—
Product(E)-3-(4-tert-Butyl-phenyl)-N-phenyl-acrylamideHCID 5885566—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a 10 mL glass vial was added 4-tert-butyl-trans-cinnamic acid (200 mg, 0.98 mmol, EMKA-Chemie) followed by CH2Cl2 (5 mL), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (225 mg, 1.17 mmol, Bachem) and aniline (98 uL, 100 mg, 1.08 mmol, Aldrich). The reaction mixture was magnetically stirred at 25° C. for 24 h. EtOAc was added (60 mL) and the mixture washed successively with 1 N NaOH (2×20 mL), 1 N HCl (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 white crystals. MP 141° C. MS (ESI, pos. ion) m/z: 280 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582657B2
Source datasetuspto-grants-2009_09
ORD IDord-0da29454cdb04e7698bda38a4d2fc137
Source noteuspto-grants-2009_09