HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 236905
Notes
Print preview

Reaction equation

HRID 236905 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.

Workup

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

Sources & evidence

ORD record
ord-30c05e65b6b047779a9e7c15349e4156
Source dataset
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04158734

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes