Acetic Acid → Neramexane

HRID 2364111Notes

Reaction equation

HRID 2364111 reaction equation
O[C:2]1([CH3:12])[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4]([CH3:11])([CH3:10])[CH2:3]1.[C-]#[N:14].[Na+].C(O)(=O)C.S(=O)(=O)(O)O>O.CCOCC.[OH-].[Na+]>[CH3:8][C:6]1([CH3:9])[CH2:7][C:2]([NH2:14])([CH3:12])[CH2:3][C:4]([CH3:11])([CH3:10])[CH2:5]1

Participants

8

Procedure

To a vigorously stirred solution of 1-hydroxy-1,3,3,5,5-pentamethylcyclohexane (3.4 g; 20 mmol) and sodium cyanide (1.96 g; 40 mmol; 2 eq.) and 5 ml acetic acid, 95% sulfuric acid (5.3 ml; 100 mmol; 5.15 eq) are added during 1 hour keeping the temperature at 10° C. for 30 min, and then allowing the mixture to reach ambient temperature. After stirring at ambient temperature for 17 hours, the mixture is diluted with 20 ml ice water. Subsequently, the mixture is refluxed with stirring for 10 hours, cooled to ambient temperature, diluted with 40 ml water and 20 ml ether and neutralized with 20% aqueous sodium hydroxide until a pH of 10. The organic phase is separated and dried. Dry hydrogen chloride is passed through the solution until the ether becomes acidic. Solvent is removed and the residue is washed with ether to give 2.24 g Neramexane in the form of its hydrochloride.

Workup

  1. customat 10° C.
  2. customfor 30 min
  3. customto reach ambient temperature
  4. temperatureSubsequently, the mixture is refluxed
  5. stirringwith stirring for 10 hours
  6. temperaturecooled to ambient temperature
  7. customThe organic phase is separated
  8. customdried
  9. customSolvent is removed
  10. washthe residue is washed with ether

Sources & evidence

ORD record
ord-3e18a55207f645e3a8ab18e78247ae16
Source dataset
uspto-grants-2014_04
Patent number
US08692021B2

Reaction notes

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