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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270698Generated: October 25, 2026

2-Aminobenzaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamide

https://huagongshe.com/reaction/270698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzaldehydeHCID 68255—
Reactant2,6-Dichloro-3-nitrophenylacetic acidHCID 54265437—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
Product2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamideHCID 5983388288.6%

Reaction Steps

A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (0.90 g, 3.35 mmol) in thionyl chloride (15 mL) is refluxed for one hour. The solvent is removed by concentration and dry toluene is added to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (30 mL) is added (drop-wise) a solution of 2-aminobenzaldehyde (0.365 g, 3.02 mmol) in dichloromethane (5.0 mL). The mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with EtOAc and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product (0.94 g, 88.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449582B2
Source datasetuspto-grants-2008_11
ORD IDord-85921cc9266e4e75939cb8df0dbc30ea
Source noteuspto-grants-2008_11