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Acetic Acid → 1-Methyl-2-propyl-3,5diethylpyridinium acetate

HRID 27257
Notes
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Reaction equation

HRID 27257 reaction equation
[CH3:1][N:2]1[CH:7]=[C:6]([CH2:8][CH3:9])[CH:5]=[C:4]([CH2:10][CH3:11])[CH:3]1[CH2:12][CH2:13][CH3:14].[C:15]([OH:18])(=[O:17])[CH3:16]>O>[C:15]([O-:18])(=[O:17])[CH3:16].[CH3:1][N+:2]1[CH:7]=[C:6]([CH2:8][CH3:9])[CH:5]=[C:4]([CH2:10][CH3:11])[C:3]=1[CH2:12][CH2:13][CH3:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 176Acetic AcidHCID 23344437HCID 23344437, compound

Product 1

HCID 127174231-Methyl-2-propyl-3,5diethylpyridinium acetateYield 96%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A sample of 38.6 g of 1-methyl-2-propyl-3,5-diethyl 1,2-dihydropyridine was added to a mixture of 12 grams of acetic acid and 26 grams of water. The mixture was stirred and air was introduced for 18 hours. The resulting aqueous phase was evaporated under diminished pressure to yield 48.2 grams of 1-methyl-2-propyl-3,5 diethylpyridinium acetate, identical to the product described in example 1.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. additionair was introduced for 18 hours
  2. customThe resulting aqueous phase was evaporated under diminished pressure

Sources & evidence

ORD record
ord-6fbdda1558e44c919b4010b19ba315a6
Source dataset
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04220785

Reaction notes

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