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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050198Generated: October 30, 2026

3,5-Dichloroaniline → HCID 23333926, compound

https://huagongshe.com/reaction/2050198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DichloroanilineHCID 12281—
ReactantMethyl 4-FormylbenzoateHCID 15294—
SolventEthanolHCID 702—
ProductHCID 23333926HCID 23333926—

Reaction Steps

p-Carbomethoxybenzaldehyde (0.20 moles) was treated with 3,5-dichloroaniline (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 5 minutes. 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 85% ethanol gave N-(p-carbomethoxybenzylidene)-3,5-dichloroaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200648
Source datasetuspto-grants-1980_04
ORD IDord-110f18219009481a92af082b00b32451
Source noteuspto-grants-1980_04