Hydrogen Bromide → 1-(2-Bromoethyl)piperidine hydrobromide

HRID 484829Notes

Reaction equation

HRID 484829 reaction equation
O([CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)C1C=CC=CC=1.[BrH:16]>C(Cl)(Cl)Cl>[BrH:16].[Br:16][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 120169Piperidine, 1-(2-phenoxyethyl)-

Product 1

HCID 124407831-(2-Bromoethyl)piperidine hydrobromideYield 79%

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

15 g of the 1-(2-phenoxyethyl)piperidine thus obtained was reacted with 30 ml of 40% hydrobromic acid at 150° C. for 7 hours with stirring. The reaction solution was cooled, added with 20 ml of chloroform and then the chloroform layer was separated. The hydrobromic acid layer was condensed under reduced pressure and the residue was recrystallized from 5 ml of ethyl alcohol to give 15.1 g of 1-(2-bromoethyl)piperidine hydrobromide having a melting point of 89° C. to 91° C. in a yield of 79%.

Workup

  1. temperatureThe reaction solution was cooled
  2. customthe chloroform layer was separated
  3. customcondensed under reduced pressure
  4. customthe residue was recrystallized from 5 ml of ethyl alcohol

Sources & evidence

ORD record
ord-76865f72ee6344dd80d17dc3804f5940
Source dataset
uspto-grants-1985_08
Patent number
US04533731

Reaction notes

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