3,4-Dichlorobenzoic acid → HCID 178465960, compound

HRID 227313Notes

Reaction equation

HRID 227313 reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[Cl:17][C:18]1[CH:19]=[C:20]([CH:24]=[CH:25][C:26]=1[Cl:27])[C:21](O)=[O:22]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:21]([C:20]2[CH:24]=[CH:25][C:26]([Cl:27])=[C:18]([Cl:17])[CH:19]=2)[OH:22])[C:5]1=[O:16])(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 58173,4-Dichlorobenzoic acidHCID 210845601,5-Diacetyl-2-indolinone

Product 1

HCID 178465960HCID 178465960, compound

Procedure

Prepared from 1,5-diacetyl-2-indolinone and 3,4-dichlorobenzoic acid

Sources & evidence

ORD record
ord-0373182e20ce4d71a7462ca759fe9849
Source dataset
uspto-grants-2009_07
Patent number
US07560480B2

Reaction notes

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