Sodium Hydroxide → HCID 18925574, compound
Reaction equation
[CH3:1][C:2]12[CH2:29][CH:5]([C:6]3([CH3:28])[C:10]1([CH3:11])[C:9]1[CH:12]=[C:13]([C:16]([C:18]4[CH:27]=[CH:26][C:21]([C:22]([O:24]C)=[O:23])=[CH:20][CH:19]=4)=[O:17])[CH:14]=[CH:15][C:8]=1[O:7]3)[CH2:4][CH2:3]2.[OH-].[Na+]>CO>[CH3:1][C:2]12[CH2:29][CH:5]([C:6]3([CH3:28])[C:10]1([CH3:11])[C:9]1[CH:12]=[C:13]([C:16]([C:18]4[CH:19]=[CH:20][C:21]([C:22]([OH:24])=[O:23])=[CH:26][CH:27]=4)=[O:17])[CH:14]=[CH:15][C:8]=1[O:7]3)[CH2:4][CH2:3]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.52 g (6.44 mmol) of the ester obtained in Example 8, in solution in 30 ml of methanol, were treated with 2.5 g of sodium hydroxide and heated at reflux for 3 hours. After the same treatment as in Example 7, followed by recrystallization from hexane, 2.35 g (97%) of the expected coompound, melting at 262°-264° C., are isolated.
Workup
- temperatureheated
- temperatureat reflux for 3 hours
- customAfter the same treatment as in Example 7, followed by recrystallization from hexane, 2.35 g (97%) of the expected coompound, melting at 262°-264° C.
- customare isolated
Sources & evidence
- ORD record
- ord-4c3bf28ed02a4cb4b2697217059896c3
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05702710
Reaction notes
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