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

Styrene Oxide → HCID 10662045, compound

HRID 596617
Notes
Print preview

Reaction equation

HRID 596617 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][NH2:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[CH2:14]1[O:22][CH:15]1[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>O1CCCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][NH:13][CH2:14][CH:15]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[OH:22])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7276Styrene OxideHCID 8421Homoveratrylamine

Product 1

HCID 10662045HCID 10662045, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A mixture of 100 g. (0.55 mol) of 3,4-dimethoxyphenylethylamine and 66.2 g. (0.55 mol) of styrene oxide in 200 ml. of tetrahydrofuran is refluxed overnight. The solvent is removed in vacuo, about 500 ml. of n-butyl chloride is added and the mixture cooled slightly. Filtration furnishes N-[2-(3,4-dimethoxyphenyl)ethyl]-2-phenyl-2-hydroxyethylamine, m.p. 92°-93° C.

Workup

  • additionA mixture of 100 g
  • customThe solvent is removed in vacuo, about 500 ml
  • additionof n-butyl chloride is added
  • temperaturethe mixture cooled slightly
  • filtrationFiltration
  • Sources & evidence

    ORD record
    ord-b95514401995467184049839ff0bc30b
    Source dataset
    uspto-grants-1977_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04011319

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes