12-Hydroxy-8-(methanesulfonyl)heptadecanoic acid → HCID 21317552, compound
Reaction equation
[CH3:1][S:2]([CH:5]([CH2:15][CH2:16][CH2:17][CH:18]([OH:24])[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH2:6][CH2:7][CH2:8][CH2:9]CCC(O)=O)(=[O:4])=[O:3].CSC(CCCC(O)CCCCC)CCCC[O:32][CH2:33][C:34]([OH:36])=[O:35]>>[CH3:1][S:2]([CH:5]([CH2:15][CH2:16][CH2:17][CH:18]([OH:24])[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH2:6][CH2:7][CH2:8][CH2:9][O:32][CH2:33][C:34]([OH:36])=[O:35])(=[O:3])=[O:4]Participants
3
Procedure
This compound is prepared essentially by the method described in Example 2 except that the 8-methylthio-12-hydroxyheptadecanoic acid of Example 2 is replaced by 5-methylthio-9-hydroxytetradecyloxyacetic acid. The product is purified by chromatography on silica gel and is obtained as a very viscous yellowish oil.
Workup
- customThis compound is prepared essentially by the method
- customThe product is purified by chromatography on silica gel
- customis obtained as a very viscous yellowish oil
Sources & evidence
- ORD record
- ord-ac73e247c5a846ec93ffbbfd7f468cb7
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04128564
Reaction notes
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