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Ethanol → 2-(6-Carbethoxyoctyl)-2-cyclopentenone

HRID 1576562
Notes
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Reaction equation

HRID 1576562 reaction equation
[C:1]([CH:4]([CH2:16][CH3:17])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[C:11](=[O:15])[CH2:12][CH2:13][CH:14]=1)([OH:3])=[O:2].S(Cl)(Cl)=O.[CH2:22](O)[CH3:23]>>[C:1]([CH:4]([CH2:16][CH3:17])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[C:11](=[O:15])[CH2:12][CH2:13][CH:14]=1)([O:3][CH2:22][CH3:23])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 217678162-(6-Carboxyoctyl)-2-cyclopentenone

Product 1

HCID 132897872-(6-Carbethoxyoctyl)-2-cyclopentenone

Procedure

Treatment of 2-(6-carboxyoctyl)-2-cyclopentone (Example 131) with thionyl chloride and then treatment of the acid chloride with ethanol in the manner described in Example 456 gives an amber oil. The oil is placed on a magnesia-silica gel column and eluted with 3:1 benzene:ether. The solvent is removed and the residue is distilled, b.p. 122°C. (0.06 mm).

Workup

  1. customgives an amber oil
  2. washeluted with 3:1 benzene
  • customThe solvent is removed
  • distillationthe residue is distilled
  • Sources & evidence

    ORD record
    ord-9282ce4a2e184f19b8d3adbde24cb7db
    Source dataset
    uspto-grants-1976_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US03981868

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes