12-Bromo-1-dodecanol → 12-(4-Methylphenyl)sulfonyl-1-tetrahydropyranyloxydodecane
Reaction equation
C(SC1C=CC(C=CC2C=CC(S(CCC[CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][OH:45])(=O)=O)=CC=2)=CC=1)CCCCCCCCCCCCCCCCC.[CH3:46][C:47]1[CH:52]=[CH:51][C:50]([S:53]([CH2:56][CH2:57][CH2:58]OC2CCCCO2)(=[O:55])=[O:54])=[CH:49][CH:48]=1.BrCCC[CH2:70][CH2:71][CH2:72][CH2:73][CH2:74][CH2:75][CH2:76][CH2:77][CH2:78][OH:79]>>[CH3:46][C:47]1[CH:48]=[CH:49][C:50]([S:53]([CH2:56][CH2:57][CH2:58][CH2:70][CH2:71][CH2:72][CH2:73][CH2:74][CH2:75][CH2:76][CH2:77][CH2:78][O:79][CH:40]2[CH2:41][CH2:42][CH2:43][CH2:44][O:45]2)(=[O:54])=[O:55])=[CH:51][CH:52]=1Participants
4
Procedure
4-octadecylthio-4'-[(1-hydroxy)-8-octylsulfonyl]stilbene. 4n) As described in Examples 1a and 2a 12-bromo-1-dodecanol gives 12-(4-methylphenyl)sulfonyl-1-tetrahydropyranyloxydodecane. Using this compound similarly gives:
Sources & evidence
- ORD record
- ord-35e7ccac4c224c71a3f4de7f53a9270b
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05517350
Reaction notes
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