HCID 21556734, compound → HCID 21556732, compound

HRID 267293Notes

Reaction equation

HRID 267293 reaction equation
[Cl:1][C:2]1[C:7]([CH:8]([CH3:10])[CH3:9])=[CH:6][C:5]([SH:11])=[C:4]([CH:12]([CH3:14])[CH3:13])[CH:3]=1.Br[C:16]1C(C(C)C)=CC(S)=C(C(C)C)C=1>>[CH3:16][S:11][C:5]1[CH:6]=[C:7]([CH:8]([CH3:9])[CH3:10])[C:2]([Cl:1])=[CH:3][C:4]=1[CH:12]([CH3:14])[CH3:13]

Participants

3

Reactant 2

HCID 21556734HCID 21556734, compoundHCID 215567424-Bromo-2,5-di(propan-2-yl)benzene-1-thiol

Product 1

HCID 21556732HCID 21556732, compound

Procedure

4-Chloro-2,5-diisopropylphenyl methyl sulfide was prepared using the procedure of Example 1C except that 4-chloro-2,5-diisopropylbenzenethiol was substituted for the 4-bromo-2,5-diisopropylbenzenethiol. The resulting product had a boiling point of 88°C at 0.35 mm Hg.

Sources & evidence

ORD record
ord-0b045442bd4949c3b258dc89f471f686
Source dataset
uspto-grants-1976_03
Patent number
US03941826

Reaction notes

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