HCID 21556733, compound → HCID 21556735, compound

HRID 267296Notes

Reaction equation

HRID 267296 reaction equation
[Cl:1][C:2]1[C:7]([CH2:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([S:12](Cl)(=O)=O)=[C:4]([CH:16]([CH3:18])[CH3:17])[CH:3]=1.BrC1C(C(CC)C)=CC(S(Cl)(=O)=O)=C(C(CC)C)C=1>>[Cl:1][C:2]1[C:7]([CH2:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([SH:12])=[C:4]([CH:16]([CH3:18])[CH3:17])[CH:3]=1

Participants

3

Reactant 2

HCID 21556733HCID 21556733, compoundHCID 21556739HCID 21556739, compound

Product 1

HCID 21556735HCID 21556735, compound

Procedure

4-Chloro-2-isopropyl-5-isobutylbenzenethiol was prepared using the procedure of Example 2B except that 4-chloro-2-isopropyl-5-isobutylbenzenesulfonyl chloride was substituted for the 4-bromo-2,5-di-sec-butylbenzenesulfonyl chloride. The resulting product had a boiling point of 77°C at 0.1 mm Hg.

Sources & evidence

ORD record
ord-f57adcb7d93b4dbe95a71a16a5799e4a
Source dataset
uspto-grants-1976_03
Patent number
US03941826

Reaction notes

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