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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963336Generated: October 30, 2026

Triethylamine → 4-Amino-5-chloro-N,2-dimethoxy-N-methylbenzamide

https://huagongshe.com/reaction/963336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Amino-5-chloro-N,2-dimethoxy-N-methylbenzamideHCID 1908184982%

Reaction Steps

4-Amino-5-chloro-2-methoxybenzoic acid (10.1 g, 50 mmol) was dissolved in DMF (50 mL). Carbonyldiimidazole (8.9 g, 55 mmol) was added to the solution and the mixture was stirred for 15 minutes. Triethylamine (7 mL, 5.1 g, 50 mmol) and N,O-dimethylhydroxylamine hydrochloride (6.3 g, 65 mmol) were added and the mixture was stirred for 12 hours. The mixture was then diluted with water and extracted into ethyl acetate. The ethyl acetate extract was washed with 5% HCl, with water, and then with brine. The extract was dried over sodium sulfate and then evaporated. Crystallization from ethyl acetate gave N-methoxy-N-methyl-4-amino-5-chloro-2-methoxybenzamide (10 g, 41 mmol), m.p. 134°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763458
Source datasetuspto-grants-1998_06
ORD IDord-c372688583df4b249a171ef2e712d810
Source noteuspto-grants-1998_06