HCID 21556733, compound → HCID 21556744, compound

HRID 267294Notes

Reaction equation

HRID 267294 reaction equation
[Br:1][C:2]1[C:7]([CH:8]([CH3:10])[CH3:9])=[CH:6][C:5]([S:11](Cl)(=O)=O)=[C:4]([CH:15]([CH2:17][CH3:18])[CH3:16])[CH:3]=1.BrC1C(C(CC)C)=CC(S(Cl)(=O)=O)=C(C(CC)C)C=1>>[Br:1][C:2]1[C:7]([CH:8]([CH3:10])[CH3:9])=[CH:6][C:5]([SH:11])=[C:4]([CH:15]([CH2:17][CH3:18])[CH3:16])[CH:3]=1

Participants

3

Reactant 2

HCID 21556733HCID 21556733, compoundHCID 21556748HCID 21556748, compound

Product 1

HCID 21556744HCID 21556744, compound

Procedure

4-Bromo-2-sec-butyl-5-isopropylbenzenethiol was prepared using the procedure of Example 2B except that 4-bromo-2-sec-butyl-5-isopropylbenzenesulfonyl chloride was substituted for the 4-bromo-2,5-di-sec-butylbenzenesulfonyl chloride. The resulting product had a boiling point of 110°C at 0.35 mm Hg.

Sources & evidence

ORD record
ord-ee1a545f4ef24e71981f3c84cc7b163c
Source dataset
uspto-grants-1976_03
Patent number
US03941826

Reaction notes

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