4-Chloro-3-nitrobenzaldehyde → HCID 135527084, compound

HRID 1862373Notes

Reaction equation

HRID 1862373 reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][C:5](=O)[CH2:4][C:3]1=[O:9].[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][C:13]=1[N+:20]([O-:22])=[O:21].[NH2:23][C:24]1[CH:28]=[CH:27][NH:26][N:25]=1>>[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]2[C:4]3[C:3](=[O:9])[C:2]([CH3:10])([CH3:1])[CH2:7][CH2:6][C:5]=3[NH:23][C:24]3=[CH:28][CH:27]=[N:26][N:25]23)=[CH:14][C:13]=1[N+:20]([O-:22])=[O:21]

Participants

4

Reactant 3

HCID 855054-Chloro-3-nitrobenzaldehydeHCID 1363601,3-Cyclohexanedione, 4,4-dimethyl-HCID 178418806HCID 178418806, compound

Product 1

HCID 135527084HCID 135527084, compound

Procedure

4,4-Dimethyl-1,3-cyclohexanedione, 4-chloro-3-nitrobenzaldehyde and 3-aminopyrazole were processed as described in General Procedure A to provide the title compound.

Sources & evidence

ORD record
ord-ee83ebdd95544baf879b24560ee75a79
Source dataset
uspto-grants-2003_03
Patent number
US06538000B1

Reaction notes

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