Benzaldehyde → 43056-25-3

HRID 261830Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH:10](=[N:5][C:4]1[CH:6]=[CH:7][C:8]([Cl:9])=[C:2]([Cl:1])[CH:3]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

Reactant 2

HCID 240Benzaldehyde

HCID 72573,4-Dichloroaniline

Product 1

HCID 91402843056-25-3

Procedure

Equimolar amounts of 3,4-dichloroaniline and benzaldehyde are stirred together at room temperature to give a nearly quantitative yield of N-(benzylidene)-3,4-dichloroaniline that melts at 62°-5° C. upon recrystallization from ethanol.

Sources & evidence

ORD record: ord-557afe8a364847c6927402684f61158f
Source dataset: uspto-grants-1979_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04152452

Reaction notes

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