Sodium Hydroxide → 4-[[trans-2-(1-Piperidyl)cyclohexyl]oxy]benzoic acid
Reaction equation
[N:1]1([C@@H:7]2[CH2:12][CH2:11][CH2:10][CH2:9][C@H:8]2[O:13][C:14]2[CH:23]=[CH:22][C:17]([C:18]([O:20]C)=[O:19])=[CH:16][CH:15]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[Na+]>CO.C1COCC1>[N:1]1([C@@H:7]2[CH2:12][CH2:11][CH2:10][CH2:9][C@H:8]2[O:13][C:14]2[CH:15]=[CH:16][C:17]([C:18]([OH:20])=[O:19])=[CH:22][CH:23]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A solution of methyl 4-[[trans-2-(1-piperidyl)cyclohexyl]oxy]benzoate (Part B) (2.232 g, 7.03 mmol) and 10.6 mL (10.6 mmol) of 1.0 N NaOH in 60 mL of 1:1 mixture of MeOH/THF was stirred at 80° C. for 20 h. The mixture was then cooled to room temperature, stirred for additional 7 h, and concentrated under reduced pressure. The residue was dissolved in 50 mL of 1.0 N HCl. This solution was extracted with 200 mL of EtOAc. The organic layer was washed with 200 mL of water. The combined aqueous layers were cooled to 0° C. and neutralized with 15 mL of 2.0 N NaOH. They were then concentrated under reduced pressure and the residue was taken up in 10% MeOH in CH2Cl2 and then filtered. The filtrate was concentrated and the residue was dried over P2O5 in a vacuum oven at 55° C.
Workup
- temperatureThe mixture was then cooled to room temperature
- stirringstirred for additional 7 h
- concentrationconcentrated under reduced pressure
- dissolutionThe residue was dissolved in 50 mL of 1.0 N HCl
- extractionThis solution was extracted with 200 mL of EtOAc
- washThe organic layer was washed with 200 mL of water
- temperatureThe combined aqueous layers were cooled to 0° C. and neutralized with 15 mL of 2.0 N NaOH
- concentrationThey were then concentrated under reduced pressure
- filtrationfiltered
- concentrationThe filtrate was concentrated
- dry with materialthe residue was dried over P2O5 in a vacuum oven at 55° C.
Sources & evidence
- ORD record
- ord-1f3cdf56e6164abeb167d092ef9a8cfb
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265575B1
Reaction notes
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