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

Anisole → HCID 13425547, compound

HRID 1249324
Notes
Print preview

Reaction equation

HRID 1249324 reaction equation
F[B-](F)(F)F.[N+:6]([C:9]1[CH:10]=[C:11]([N+]#N)[CH:12]=[CH:13][CH:14]=1)([O-:8])=[O:7].C([O-])(=O)C.[K+].[C:22]1([O:28][CH3:29])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[CH3:29][O:28][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:11]1[CH:12]=[CH:13][CH:14]=[C:9]([N+:6]([O-:8])=[O:7])[CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 7519AnisoleHCID 517044Potassium AcetateHCID 11665863HCID 11665863, compound

Product 1

HCID 13425547HCID 13425547, compound

Procedure

Anisole (400 mL) and 3-nitrobenzenediazonium tetrafluoroborate (54.5 g, 0.23 mol) were placed in a 1-L flask and stirred mechanically. Potassium acetate (49.0 g, 0.5 mol) was added in one portion. The mixture turned red and warmed slightly. Stirring was continued 12 h., then the solution was filtered and the anisole evaporated in vacuo. Column chromatography of the residue (alumina, 0-10% ether/hexane, first yellow band) and recrystallization (95% EtOH) provided pure 2-methoxy-3'-nitrobiphenyl: 18 g (35%); mp 68°-69° C.

Workup

  • temperaturewarmed slightly
  • stirringStirring
  • filtrationthe solution was filtered
  • customthe anisole evaporated in vacuo
  • customColumn chromatography of the residue (alumina, 0-10% ether/hexane, first yellow band) and recrystallization (95% EtOH)
  • Sources & evidence

    ORD record
    ord-d18e8faf045b4f39a44730e00eb674e4
    Source dataset
    uspto-grants-1986_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04631119

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes