Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852247Generated: October 30, 2026

Diethylamine → N,N-diethyl-4-methoxy-2-methyl-benzamide

https://huagongshe.com/reaction/1852247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant4-Methoxy-2-methylbenzoic acidHCID 597216—
SolventWaterHCID 962—
SolventThionyl ChlorideHCID 24386—
ProductN,N-diethyl-4-methoxy-2-methyl-benzamideHCID 1105321857.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-methoxy-2-methylbenzoic acid (3.0 g, 18.05 mmol) was taken in thionyl chloride (20 ml) and refluxed for 1 h at 80° C. The reaction mixture was evaporated under reduced pressure. Under nitrogen the crude was quenched with diethyl amine (1.870 ml, 18.05 mmol) slowly under cooling conditions. The reaction mixture was dissolved in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (20% ethyl acetate in pet ether) to get desired compound (2.3 g, 54.7%) as oil. 1H NMR (400 MHz, DMSO-d6): δ ppm 7.06-7.04 (d, J=8 Hz, 1H), 6.79 (s, 1H), 6.78-6.76 (d, J=8 Hz, 1H), 3.75 (s, 3H), 3.43 (br, s, 2H), 3.06-3.05 (m, 2H), 2.16 (s, 3H), 1.14 (d, J=8 Hz, 3H), 0.95 (d, J=8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957203B2
Source datasetuspto-grants-2015_02
ORD IDord-0cadb5fb05b54698b318f40ed9189234
Source noteuspto-grants-2015_02