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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167657Generated: October 25, 2026

Ethylamine → N-ethyl-2-chloro-5-nitrobenzamide

https://huagongshe.com/reaction/1167657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-nitrobenzoic acidHCID 17287—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventTetrahydrofuranHCID 8028—
ProductN-ethyl-2-chloro-5-nitrobenzamideHCID 438019545.5%

Reaction Steps

2-Chloro-5-nitrobenzoic acid (20 g, 100 mmol) in THF (200 mL) was treated with carbonyldiimidazole (CDI) (17.8 g, 110 mmol) and triethylamine (16 mL, 110 mmol) at room temperature. After 1 hr, a solution of ethylamine (70% in water, 10 mL) was added and the mixture was stirred for 18 h. Solvent was removed by evaporation and the residue was dissolved in methylene chloride, washed with 3% KOH solution followed by water (three times) until the aqueous phase extracts were colorless. The organic phase was dried over MgSO4, filtered, and the filtrate was concentrated to provide 10.4 g of N-ethyl-2-chloro-5-nitrobenzamide as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620827B2
Source datasetuspto-grants-2003_09
ORD IDord-895a572207c54c86ab1669f4b9f811b0
Source noteuspto-grants-2003_09