o-Toluenesulfonyl chloride → HCID 53929232, compound

HRID 1389737Notes

Reaction equation

HRID 1389737 reaction equation
[Br:1][C:2]1[C:7]([O:8][S:9]([C:12]2[C:13](C)=[CH:14][CH:15]=[CH:16][CH:17]=2)(=[O:11])=[O:10])=[C:6]([Br:19])[C:5]([Br:20])=[C:4]([Br:21])[C:3]=1[Br:22].[C:23]1(C)C(S(Cl)(=O)=O)=CC=CC=1>>[Br:1][C:2]1[C:7]([O:8][S:9]([C:12]2[CH:13]=[CH:14][C:15]([CH3:23])=[CH:16][CH:17]=2)(=[O:10])=[O:11])=[C:6]([Br:19])[C:5]([Br:20])=[C:4]([Br:21])[C:3]=1[Br:22]

Participants

3

Reactant 2

HCID 8623o-Toluenesulfonyl chlorideHCID 54106749HCID 54106749, compound

Product 1

HCID 53929232HCID 53929232, compound

Procedure

The o-toluenesulfonic acid pentabromophenyl ester can be prepared in the same manner by using the same molar amount of o-toluenesulfonyl chloride instead of the para compound.

Sources & evidence

ORD record
ord-9ed43161d06549ecacd90f38c62174e8
Source dataset
uspto-grants-1981_01
Patent number
US04246188

Reaction notes

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