4-Hydroxybenzoic Acid → HCID 178524492, compound
Reaction equation
[C:1]1([Sb:7](=O)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=1>>[OH:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([O-:28])=[O:27])=[CH:24][CH:23]=1.[OH:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([O-:28])=[O:27])=[CH:24][CH:23]=1.[C:14]1([Sb+2:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1Participants
3
Procedure
Triphenyl antimony oxide was reacted with p-hydroxybenzoic acid to yield triphenyl antimony di(p-hydroxybenzoate). ##SPC6##
Sources & evidence
- ORD record
- ord-99fa50cf6497414786bae6b9746be90b
- Source dataset
- uspto-grants-1976_02
- Patent number
- US03939190
Reaction notes
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