Hydrogen Sulfide → 6-tert-Butyl-2,4-dimethyl-3-(sulfanylmethyl)phenol
Reaction equation
[CH3:1][C:2]1[C:7]([CH2:8]Cl)=[C:6]([CH3:10])[CH:5]=[C:4]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:3]=1[OH:15].C(N(CC)CC)C.[SH2:23]>O1CCCC1>[CH3:1][C:2]1[C:7]([CH2:8][SH:23])=[C:6]([CH3:10])[CH:5]=[C:4]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:3]=1[OH:15]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
This material was synthesized according to the procedure of Song (Song, J. U.S. Pat. No. 3,810,929) using 2,4-dimethyl-3-chloromethyl-6-t-butylphenol (160.8 g, 0.71 m), triethylamine (80 g), tetrahydrofuran (200 ml) and excess hydrogen sulfide. This afforded upon work-up a slightly yellow odorous oil.
Workup
- customThis material was synthesized
- customThis afforded upon work-up a slightly yellow odorous oil
Sources & evidence
- ORD record
- ord-da0fe72c90f44c90815efb44cbb62490
- Source dataset
- uspto-grants-1979_07
- Patent number
- US04163008
Reaction notes
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