2-Chloroethyl methyl sulfide → (Z)-4-[4-(2-Methylsulfanylethoxy)phenyl]-3,4-diphenyl-but-3-en-1-ol
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[C:9]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:10][CH2:11][OH:12])=[CH:4][CH:3]=1.[CH3:25][S:26][CH2:27][CH2:28]Cl>>[CH3:25][S:26][CH2:27][CH2:28][O:1][C:2]1[CH:3]=[CH:4][C:5](/[C:8](/[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[C:9](\[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)/[CH2:10][CH2:11][OH:12])=[CH:6][CH:7]=1Participants
3
Procedure
The compound is prepared by using the method described in the example 1a starting from 4-(4-hydroxyphenyl)-3,4-diphenyl-but-3-en-1-ol (preparation described in U.S. Pat. No. 4,996,225) and 2-chloroethyl methyl sulfide.
Workup
- customThe compound is prepared
- custompreparation
Sources & evidence
- ORD record
- ord-b9edb49a1db74599ab9f52df0c1b9108
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06875775B2
Reaction notes
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