HCID 21556735, compound → HCID 21556736, compound

HRID 267297Notes

Reaction equation

HRID 267297 reaction equation
[Cl:1][C:2]1[C:7]([CH2:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([SH:12])=[C:4]([CH:13]([CH3:15])[CH3:14])[CH:3]=1.Br[C:17]1C(C(C)C)=CC(S)=C(C(C)C)C=1>>[CH3:17][S:12][C:5]1[CH:6]=[C:7]([CH2:8][CH:9]([CH3:11])[CH3:10])[C:2]([Cl:1])=[CH:3][C:4]=1[CH:13]([CH3:15])[CH3:14]

Participants

3

Reactant 2

HCID 21556735HCID 21556735, compoundHCID 215567424-Bromo-2,5-di(propan-2-yl)benzene-1-thiol

Product 1

HCID 21556736HCID 21556736, compound

Procedure

4-Chloro-2-isopropyl-5-isobutylphenyl methyl sulfide was prepared using the procedure of Example 1C except that 4-chloro-2-isopropyl-5-isobutylbenzenethiol was substituted for the 4-bromo-2,5-diisopropylbenzenethiol. The resulting product had a boiling point of 89°C at 0.08 mm Hg.

Sources & evidence

ORD record
ord-1f977b7975ee46609ed043c140b23b97
Source dataset
uspto-grants-1976_03
Patent number
US03941826

Reaction notes

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