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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237515Generated: October 26, 2026

Dimethylamine → N,N,3,5-Tetramethyl-4-nitrobenzamide

https://huagongshe.com/reaction/237515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,5-Dimethyl-4-nitrobenzoic acidHCID 249413—
SolventTetrahydrofuranHCID 8028—
ProductN,N,3,5-Tetramethyl-4-nitrobenzamideHCID 86697177—

Reaction Steps

1,1′-Carbonyldiimidazole (914 mg) is added to a solution of 3,5-dimethyl-4-nitrobenzoic acid (1 g) in tetrahydrofuran (10 mL). The mixture is stirred for 3 hours at room temperature, dimethylamine (7.7 mL, 2 M in tetrahydrofuran) is added and the mixture is stirred for further 30 minutes. After concentration the mixture is diluted with ethyl acetate and washed with hydrochloric acid (0.2 M), saturated aqueous NaHCO3 solution and brine. The organic phase is dried (Na2SO4) and concentrated to give the title compound. Yield: 1 g; LC (method 20): tR=5.11 min; Mass spectrum (ESI+): m/z=223 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642585B2
Source datasetuspto-grants-2014_02
ORD IDord-8d89649c99164ec8b6e29e3e824de136
Source noteuspto-grants-2014_02