1-Chloroethyl chloroformate → 4-Benzylidenepiperidine hydrochloride

HRID 861946

Reaction equation

HRID 861946 reaction equation
C([N:8]1[CH2:13][CH2:12][C:11](=[CH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1.[Cl:21]C(OC(Cl)C)=O>ClC(Cl)C>[ClH:21].[CH:14](=[C:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

4

Procedure

There was dissolved 24.6 g (96 mmol) of 1-benzyl-4-benzylidenepiperidine in 200 ml of dichloroethane and thereto 11.1 ml (102 mmol) of 1-chloroethyl chloroformate was added dropwise under cooling with ice. The reaction solution was refluxed with heating for 30 minutes and then stirred at room temperature for 1.5 hours. The reaction solution was concentrated to 80 ml by removing the solvent under reduced pressure, thereto was added 200 ml of methanol and the obtained mixture was refluxed with heating for 12 hours. The solvent was removed under reduced pressure and to the obtained residue was added 100 ml of isopropyl ether and the precipitate was separated by filtration to obtain 8.6 g of the titled compound.

Workup

  1. temperatureunder cooling with ice
  2. temperatureThe reaction solution was refluxed
  3. temperaturewith heating for 30 minutes
  4. concentrationThe reaction solution was concentrated to 80 ml
  5. customby removing the solvent under reduced pressure
  6. additionwas added 200 ml of methanol
  7. temperaturethe obtained mixture was refluxed
  8. temperaturewith heating for 12 hours
  9. customThe solvent was removed under reduced pressure and to the obtained residue
  10. additionwas added 100 ml of isopropyl ether
  11. customthe precipitate was separated by filtration

Sources & evidence

ORD record
ord-28b37068acdc4ae4a559829bf9f32b71
Source dataset
uspto-grants-1998_02
Patent number
US05716969

Linked notes

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