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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045950Generated: October 29, 2026

Methylamine → 2-Amino-4-chloro-N-methylbenzamide

https://huagongshe.com/reaction/1045950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2-Amino-4-chlorobenzoic acidHCID 66646—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4-chloro-N-methylbenzamideHCID 1385382874.3%

Reaction Steps

Carbonyl-1,1′-diimidazole (1.70 g) was added to 2-amino-4-chlorobenzoic acid (1.50 g) in THF (22.2 mL). After stirring overnight a solution of methylamine in THF (2M, 6.6 mL) was added and the reaction stirred for 3 hours. The reaction was concentrated in vacuo and the residue dissolved in EtOAc (100 mL) and saturated aqueous sodium bicarbonate solution (50 mL). The organics were then washed with saturated aqueous sodium bicarbonate solution (50 mL) and then water (2×100 mL). The organics were extracted with 1 M HCl (4×25 mL, then 2×100 mL then 50 mL), the aqueous phase basified with potassium carbonate (˜50 g) and the organics discarded. The aqueous was then extracted with EtOAc (2×50 mL). The combined organics were dried (MgSO4, 10 g) and concentrated to give 2-amino-4-chloro-N-methylbenzamide (1.2 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569298B2
Source datasetuspto-grants-2013_10
ORD IDord-23fc722cfcc24f598c2a0eb96ea7dfa3
Source noteuspto-grants-2013_10