Sodium Hydroxide → HCID 178486047, compound

HRID 2109046Notes

Reaction equation

HRID 2109046 reaction equation
[C:1]([O:5][C:6]([N:8]([CH3:19])[C@H:9]1[CH2:14][CH2:13][C@H:12]([C:15]([O:17]C)=[O:16])[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO>[C:1]([O:5][C:6]([N:8]([CH3:19])[C@H:9]1[CH2:10][CH2:11][C@H:12]([C:15]([OH:17])=[O:16])[CH2:13][CH2:14]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 178501226HCID 178501226, compound

Product 1

HCID 178486047HCID 178486047, compoundYield 92.3%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Methyl trans-4-[(t-butoxycarbonyl)(methyl)amino]cyclohexanecarboxylate (44.78 g) obtained in Reference Example 3(1) is dissolved in methanol (300 ml), and thereto is added 2 N aqueous sodium hydroxide solution (100 ml). The mixture is then stirred at room temperature for 6 hours. The reaction solution is concentrated under reduced pressure. To the residue are added ice-water, ethyl acetate and 10% hydrochloric acid under ice-cooling, and the mixture is extracted with ethyl acetate. The organic layer is washed with water and saturated brine successively, dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. The resulting residue is suspended in a small amount of ethyl acetate, and n-hexane is poured to the mixture. The resulting crystals are collected by filtration, washed with n-hexane/diisopropyl ether several times and dried to give the title compound (39.20 g).

Workup

  1. concentrationThe reaction solution is concentrated under reduced pressure
  2. additionTo the residue are added ice-water, ethyl acetate and 10% hydrochloric acid under ice-
  3. temperaturecooling
  4. extractionthe mixture is extracted with ethyl acetate
  5. washThe organic layer is washed with water and saturated brine successively
  6. dry with materialdried over sodium sulfate
  7. customevaporated
  8. customto remove the solvent under reduced pressure
  9. additionis poured to the mixture
  10. filtrationThe resulting crystals are collected by filtration
  11. washwashed with n-hexane/diisopropyl ether several times
  12. customdried

Sources & evidence

ORD record
ord-21cc32c8d0a7477986bfb85cbc6b575d
Source dataset
uspto-grants-2009_04
Patent number
US07514449B2

Reaction notes

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