2,4-Mesitylenedisulfonyl Dichloride → HCID 86756467, compound

HRID 636775Notes

Reaction equation

HRID 636775 reaction equation
[C:1]1([SH:8])[CH:6]=[CH:5][C:4]([SH:7])=[CH:3][CH:2]=1.[C:9]1([CH3:25])[CH:14]=[C:13]([CH3:15])[C:12]([S:16]([Cl:19])(=[O:18])=[O:17])=[C:11]([CH3:20])[C:10]=1[S:21]([Cl:24])(=[O:23])=[O:22]>>[C:9]1([CH3:25])[CH:14]=[C:13]([CH3:15])[C:12]([S:16]([Cl:19])(=[O:18])=[O:17])=[C:11]([CH3:20])[C:10]=1[S:21]([Cl:24])(=[O:22])=[O:23].[C:1]1([SH:8])[CH:6]=[CH:5][C:4]([SH:7])=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 36200812,4-Mesitylenedisulfonyl DichlorideHCID 46917291,4-Benzenedithiol2×

Product 1

HCID 86756467HCID 86756467, compound

Procedure

Next, the 1,4-benzenedithiol vapor in the condensing chamber 2 was adiabatically expanded, and the introduced base particles were exposed thereto for 30 minutes. Consequently, a further polymerization reaction between 2,4-mesitylenedisulfonyl chloride and 1,4-benzenedithiol took place on the surface of the modified particles (19), forming a film of 2,4-mesitylenedisulfonylchloride-1,4-benzenedithiol co-polymer.

Sources & evidence

ORD record
ord-e1832136fd6848d2baea10330db99e2c
Source dataset
uspto-grants-2001_02
Patent number
US06194487B1

Reaction notes

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