Carbon Dioxide → 2,2,6,6-Tetramethyl-4-(chlorocarbonyloxy)piperidinium chloride

HRID 1650871Notes

Reaction equation

HRID 1650871 reaction equation
C(=O)=O.Cl.[CH3:5][C:6]1([CH3:15])[CH2:11][CH:10]([OH:12])[CH2:9][C:8]([CH3:14])([CH3:13])[NH:7]1.[C:16]([Cl:19])([Cl:18])=[O:17].N1C=CC=CC=1.[Cl-].CC1(C)CCCC[N+]1(C)C.Cl.[NH+]1C=CC=CC=1>CC(=O)CC>[Cl-:18].[CH3:5][C:6]1([CH3:15])[CH2:11][CH:10]([O:12][C:16]([Cl:19])=[O:17])[CH2:9][C:8]([CH3:14])([CH3:13])[NH2+:7]1

Participants

8

Reactant 6

HCID 280Carbon DioxideHCID 1049PyridineHCID 6371Phosgene3×HCID 189851222,2,6,6-Tetramethylpiperidinol-4 hydrochlorideHCID 21584435Pyridinium hydrochlorideHCID 23052602Tetramethylpiperidinium chloride

Product 1

HCID 867429482,2,6,6-Tetramethyl-4-(chlorocarbonyloxy)piperidinium chloride

Reagents, catalysts & solvents 1

HCID 6569Methyl Ethyl KetoneSolvent

Conditions

Temperature
80 °C

Procedure

Into a 500 ml flask equipped with a magnetic stirbar, thermometer, gas inlet adapter, dual condensers (i.e., Dry Ice condenser atop a water cooled condenser), and oil bath were placed 28.2 g (0.145 mole) of 2,2,6,6-tetramethyl-4-piperidinol hydrochloride and 250 ml of 2-butanone. The mixture was heated to reflux and 8.0 ml (0.11 mole) of condensed phosgene was allowed to evaporate into the reaction mixture cooling the mass to 73°-75° C. This was followed by pipet addition of 11.5 g (0.145 mole) of pyridine which caused an exothermic reaction raising the temperature to 80° C. An additional 10 ml (0.14 mole) of phosgene were evaporated into the system. During this time the reaction mixture cleared of initially suspended solid and then formed a precipitate. After the addition of phosgene was completed, nitrogen was bubbled into the system for 40 minutes under continued reflux. The mixture was then allowed to cool gradually overnight and then was cooled further in an ice water bath. The very hygroscopic solid was collected by filtration. The liquid was reduced to 50 ml volume by distillation at atmospheric pressure, cooled to ambient, and diluted with 100 ml of tetrahydrofuran. In this manner, more solids were obtained and isolated by filtration. The combined solids were then freed from residual solvent under high vacuum. The product was a mixture of the tetramethylpiperidinium chloride compound and pyridinium hydrochloride. This mixture was used in the next step without further purification.

Workup

  1. customInto a 500 ml flask equipped with a magnetic stirbar
  2. temperatureThe mixture was heated
  3. temperatureto reflux
  4. customto evaporate into the reaction mixture
  5. temperaturecooling the mass to 73°-75° C
  6. customan exothermic reaction
  7. customformed a precipitate
  8. customnitrogen was bubbled into the system for 40 minutes under continued reflux
  9. temperatureto cool gradually overnight
  10. temperaturewas cooled further in an ice water bath
  11. filtrationThe very hygroscopic solid was collected by filtration
  12. distillationThe liquid was reduced to 50 ml volume by distillation at atmospheric pressure
  13. temperaturecooled
  14. additiondiluted with 100 ml of tetrahydrofuran
  15. customIn this manner, more solids were obtained
  16. customisolated by filtration
  17. customThis mixture was used in the next step without further purification

Sources & evidence

ORD record
ord-c4a829849c6a4aa3bcf051f1822582c0
Source dataset
uspto-grants-1990_05
Patent number
US04925903

Reaction notes

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