Pyridine → AGN-PC-0NFGX0

HRID 2050614Notes

Reaction equation

HRID 2050614 reaction equation
[CH3:1][O:2][C:3](=[O:6])[CH2:4][Br:5].[N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>CC(C)=O>[Br-:5].[C:3]([CH2:4][N+:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([O:2][CH3:1])=[O:6]

Participants

4

Reactant 2

HCID 1049PyridineHCID 60984Methyl bromoacetate

Product 1

HCID 11075264AGN-PC-0NFGX0

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

Carbomethoxymethylpyridinium bromide is synthesized by reacting bromoacetic acid methylester with dry pyridine in acetone at room temperature. The product precipitates out as a white crystalline solid during the reaction and can be used without further purification.

Workup

  1. customat room temperature
  2. customThe product precipitates out as a white crystalline solid during the reaction
  3. customcan be used without further purification

Sources & evidence

ORD record
ord-c7b18c9294a84cfb9a3daeee9a5e08f4
Source dataset
uspto-grants-1991_05
Patent number
US05013844

Reaction notes

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