Heptanoic Acid → HCID 21436325, compound
Reaction equation
C(O)(=[O:8])CCCCCC.[OH:10][CH:11]([CH2:29][O:30][CH2:31][CH2:32][CH3:33])[CH2:12][CH2:13][N:14]1[C:18](=[O:19])[CH2:17][S:16][CH:15]1[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]([OH:28])=[O:27]>>[OH:10][CH:11]([CH2:29][O:30][CH2:31][CH2:32][CH3:33])[CH2:12][CH2:13][N:14]1[C:18](=[O:19])[CH2:17][S:16](=[O:8])[CH:15]1[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]([OH:28])=[O:27]Participants
3
Procedure
This compound is prepared essentially by the same method as described in Example 2 except that the 7-3-(3-hydroxyoctyl)-4-oxo-2-thiazolidinyl]heptanoic acid is replaced by 7-[3-(3-hydroxy-4-propoxybutyl)-4-oxo-2-thiazolidinyl]heptanoic acid. This method provides the title compound as an essentially colorless, viscous oil.
Workup
- customThis compound is prepared essentially by the same method
Sources & evidence
- ORD record
- ord-756afa306eb148ea8b3a4df93123d3a6
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04022794
Reaction notes
Loading…