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

Nonanoic Acid → Ethylene brassylate

HRID 1074628
Notes
Print preview

Reaction equation

HRID 1074628 reaction equation
C[CH:2]([CH3:4])[O-:3].[Al+3].C[CH:7]([CH3:9])[O-:8].CC(C)[O-].C(O)(=O)CCCCCCCC.[C:25]([O-:44])(=[O:43])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35]CCCCCCC.[K+]>>[C:2]1(=[O:3])[O:8][CH2:7][CH2:9][O:44][C:25](=[O:43])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:4]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 8158Nonanoic AcidHCID 11143Aluminum isopropoxideHCID 23673840Potassium Stearate

Product 1

HCID 61014Ethylene brassylateYield 89.3%

Procedure

Aluminum tripelargonate, obtained by reacting 0.5 mole aluminum isopropoxide and 1.5 mole pelargonic acid at 120° C., was combined with an equimolar amount, based on aluminum, of potassium stearate and the resulting mixed metal catalyst (1.7 weight percent) charged to a reactor with 76 g poly(ethylene brassylate). The depolymerization was conducted in the usual manner. Ethylene brassylate was obtained at a rate of 42 mls/hr. and yield of 89.3%.

Workup

  • customat 120° C.
  • additionthe resulting mixed metal catalyst (1.7 weight percent)
  • Sources & evidence

    ORD record
    ord-f7256867b5d54e138daba5f0ff39c66a
    Source dataset
    uspto-grants-1983_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04393223

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes