Salicylic Acid → HCID 86733066, compound

HRID 972182Notes

Reaction equation

HRID 972182 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][CH:28]=[CH:27][C:23]=1[C:24]([OH:26])=[O:25]>>[OH:21][C:22]1[CH:30]=[CH:29][CH:28]=[CH:27][C:23]=1[C:24]([OH:26])=[O:25].[OH:21][C:22]1[CH:30]=[CH:29][CH:28]=[CH:27][C:23]=1[C:24]([OH:26])=[O:25].[C:14]1([Sb: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]=1.[C:24]([O-:26])(=[O:25])[C:23]1[C:22](=[CH:30][CH:29]=[CH:28][CH:27]=1)[OH:21].[C:24]([O-:26])(=[O:25])[C:23]1[C:22](=[CH:30][CH:29]=[CH:28][CH:27]=1)[OH:21].[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]=1

Participants

4

Reactant 2

HCID 338Salicylic AcidHCID 78497Stibine oxide, triphenyl-

Product 2

HCID 86733066HCID 86733066, compoundHCID 178524315HCID 178524315, compound

Procedure

Triphenyl antimony oxide was reacted with o-hydroxy benzoic acid (salicylic acid) to yield triphenyl antimony di(hydroxy benzoic acid) (or triphenyl antimony disalicylate). ##STR11##

Sources & evidence

ORD record
ord-6ba0308906504e77a306c2da47ac839b
Source dataset
uspto-grants-1977_10
Patent number
US04052369

Reaction notes

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