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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893479Generated: October 30, 2026

N,N-Dimethylaniline → HCID 73947316, compound

https://huagongshe.com/reaction/1893479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 68666114HCID 68666114—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 73947316HCID 7394731680.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

8-Bromo-7-(trifluoromethyl)imidazo[1,2-a]quinoxalin-4(5H)-one (9.4 g, 0.0283 mol) is stirred under nitrogen with N,N-dimethylaniline (14.5 mL, 0.1123 mol) and phosphoryl chloride (190 mL, 2.0119 mol) at reflux (120° C.) for 1.5 hour. After cooling down to room temperature, the mixture is slowly poured in a mixture of water (2 L) and sodium hydroxide 5N (1 L) below 10° C. The mixture is extracted four times with ethyl acetate (200 mL) and the combined organic phases are washed with water (200 mL), dried over sodium sulfate and concentrated to about 100 mL. Cyclohexane (500 mL) is added at room temperature. The mixture is cooled to 0-5° C. and filtered. The cake is washed with cyclohexane and dried under vacuum to afford the title compound as a yellow solid (7.98 g, 80.4%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-1528f5aa9a924764b25fdaae60c49e56
Source noteuspto-grants-2013_08