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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049535Generated: October 26, 2026

3-Chloro-2-methylaniline → N-(p-carbomethoxybenzylidene)-2-methyl-3-chloroaniline

https://huagongshe.com/reaction/2049535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methylanilineHCID 6894—
ReactantMethyl 4-FormylbenzoateHCID 15294—
SolventEthanolHCID 702—
ProductN-(p-carbomethoxybenzylidene)-2-methyl-3-chloroanilineHCID 20342435—

Reaction Steps

p-carbomethoxybenzaldehyde (0.20 moles) was treated with 2-methyl-3-chloroaniline (0.20 moles) with vigorous stirring in a 1 liter Erlenmeyer flask. After 15 mins., 33 cc of 95% ethanol was added and the reaction mixture was stirred vigorously for an additional 45 mins. The reaction mixture was left standing at room temperature for 10 min., then it was placed in an ice bath for 0.5 hours. The crystals which formed were collected, washed with 95% ethanol, and air dried. Recrystallization from 95% ethanol gave N-(p-carbomethoxybenzylidene)-2-methyl-3-chloroaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198349
Source datasetuspto-grants-1980_04
ORD IDord-bad720b72534462c95bb429ac758e792
Source noteuspto-grants-1980_04