Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360389Generated: November 2, 2026

N,N-Dimethylaniline → HCID 15421643, compound

https://huagongshe.com/reaction/1360389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantPotassium HydroxideHCID 14797—
ReactantPropanoyl chloride, 3-bromo-HCID 84944—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
SolventAcetonitrile methylene chlorideHCID 21877088—
ProductHCID 15421643HCID 1542164371%

Reaction Steps

3-Bromopropanoyl chloride (3.13 mL, 31.0 mmol) and N,N-dimethylaniline (3.91 mL, 31.0 mmol) were dissolved in methylene chloride (30 ml), 4-trifluoromethylaniline (5 g, 31.0 mmol) was added dropwise at 0° C., and the mixture was stirred at room temperature for 2 hrs. Work-up of the reaction mixture according to a conventional method gave a crude product. The obtained crude product was dissolved in a mixed solvent (100 mL) of methylene chloride/acetonitrile (20/1), potassium hydroxide (2.28 g, 40.6 mmol) and tetrabutylammonium bromide (3.26 g, 6.76 mmol) were added, and the mixture was stirred overnight at room temperature. The solvent was evaporated and, after work-up according to a conventional method, the mixture was purified by silica gel column chromatography to give the title compound (4.6 g, 21.4 mmol, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879863B2
Source datasetuspto-grants-2011_02
ORD IDord-261d692158a84608a3c95ce1e87c256c
Source noteuspto-grants-2011_02