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

Methyl iodide → Ammonium, trimethyl(4-phenylbutyl)-, iodide

HRID 2371528
Notes
Print preview

Reaction equation

HRID 2371528 reaction equation
[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH3:3].[CH3:14][I:15]>CO>[I-:15].[CH3:1][N+:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([CH3:14])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6328Methyl iodideHCID 13546746N,N-dimethyl-4-phenylbutylamine

Product 1

HCID 43505Ammonium, trimethyl(4-phenylbutyl)-, iodide

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 287 mg of N,N-dimethyl-4-phenylbutylamine in 3 ml of absolute methanol, 505 μl of methyl iodide was added at a room temperature with stirring, and the mixture was stirred at a room temperature for 6.5 hours. The reaction mixture was concentrated under a reduced pressure, and after adding ethyl acetate allowed to stand for formation of crystal. The crystal was filtered, washed with ethyl acetate, and dried under a reduced pressure to obtain 439 mg of the title compound as a colorless crystal.

Workup

  1. stirringthe mixture was stirred at a room temperature for 6.5 hours
  2. concentrationThe reaction mixture was concentrated under a reduced pressure
  3. additionafter adding ethyl acetate
  4. filtrationThe crystal was filtered
  5. washwashed with ethyl acetate
  6. customdried under a reduced pressure

Sources & evidence

ORD record
ord-964d41e7070c4735a4c768d94607c276
Source dataset
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05093370

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes