Sodium Hydroxide → HCID 59442608, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2([C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)[CH2:11][CH2:10][C:9]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)([C:12]([OH:14])=[O:13])[CH2:8][CH2:7]2)[CH2:3][CH2:2]1.[OH-].[Na+:29]>O>[CH:1]1([CH2:4][O:5][C:6]2([C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)[CH2:7][CH2:8][C:9]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)([C:12]([O-:14])=[O:13])[CH2:10][CH2:11]2)[CH2:3][CH2:2]1.[Na+:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
185 mg of 4-cyclopropylmethoxy-4-(4-fluorophenyl)-1-phenylcyclohexanecarboxylic acid were treated with 0.5 ml of a 1 M sodium hydroxide solution and 2 ml of water and cautiously heated to 100° C. The solution became clear. The sodium salt crystallized during cooling. It was filtered off with suction and dried. 155 mg of the title compound were obtained as silvery white flakes.
Workup
- customThe sodium salt crystallized
- temperatureduring cooling
- filtrationIt was filtered off with suction
- customdried
Sources & evidence
- ORD record
- ord-37d5c57012414db0b7662ac5b4f86fae
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076324B2
Reaction notes
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