HCID 68706511, compound → HCID 17958604, compound
Reaction equation
[C:1]([C:4]1[CH:34]=[CH:33][C:7]([CH2:8][CH:9]([CH:17]=[CH:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:6][CH:5]=1)([OH:3])=[O:2].[H][H]>[Pd].C(OCC)(=O)C>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:8][CH:9]([CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:33][CH:34]=1)([OH:3])=[O:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
31.6 mg (0.07 mmol) of 6-(4-carboxybenzyl)-8-(2-heptoxyphenyl)-7-octenoic acid from Ex. 25 and 20 mg of palladium/activated carbon (10%) are added to 5 ml of ethyl acetate and, at room temperature and under atmospheric pressure, hydrogenated with hydrogen. After two hours, the mixture is filtered through Celite and concentrated under reduced pressure.
Workup
- filtrationthe mixture is filtered through Celite
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-5e565ebbee9145c6a68994e2ce7555ba
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674825B2
Reaction notes
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