Sodium Hydroxide → 4-[[trans-2-(1-Piperidyl)cyclohexyl]oxy]benzoic acid

HRID 1387001Notes

Reaction equation

HRID 1387001 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]1

Participants

4

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

  1. temperatureThe mixture was then cooled to room temperature
  2. stirringstirred for additional 7 h
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was dissolved in 50 mL of 1.0 N HCl
  5. extractionThis solution was extracted with 200 mL of EtOAc
  6. washThe organic layer was washed with 200 mL of water
  7. temperatureThe combined aqueous layers were cooled to 0° C. and neutralized with 15 mL of 2.0 N NaOH
  8. concentrationThey were then concentrated under reduced pressure
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated
  11. 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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