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Methanol → Methyl 4,4-bis(4-hydroxyphenyl)pentanoate

HRID 1456856
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1456856
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:15]2[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=2)([CH3:14])[CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:4][CH:3]=1.[CH3:22]O>>[CH3:22][O:12][C:11](=[O:13])[CH2:10][CH2:9][C:8]([C:15]1[CH:16]=[CH:17][C:18]([OH:21])=[CH:19][CH:20]=1)([C:5]1[CH:4]=[CH:3][C:2]([OH:1])=[CH:7][CH:6]=1)[CH3:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 887MethanolHCID 671744,4'-Bis(4-hydroxyphenyl)valeric acid

Produkt 1

HCID 247957Methyl 4,4-bis(4-hydroxyphenyl)pentanoate

Versuchsvorschrift

To a solution in methanol (120 mL) of 4,4-bis(4-hydroxyphenyl)pentanoic acid (Aldrich Chemical Co., 12 g, 42 mmol) was added concentrated H2 SO4 (0.5 mL) and the mixture was heated to reflux for 3 hours. After cooling to room temperature the mixture was concentrated in vacuo and dissolved in ether (300 mL). The organic layer was washed with saturated aqueous NaHCO3 (2×150 mL) and brine, dried over MgSO4, filtered, and concentrated in vacuo to provide a thick oil which was crystallized from ether/hexane to give 4,4-bis(4-hydroxyphenyl)pentanoic acid methyl ester as an off-white color solid (11.8 g, 94%), mp 130° C.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 3 hours
concentration
was concentrated in vacuo
  • dissolutiondissolved in ether (300 mL)
  • washThe organic layer was washed with saturated aqueous NaHCO3 (2×150 mL) and brine
  • dry with materialdried over MgSO4
  • filtrationfiltered
  • concentrationconcentrated in vacuo
  • customto provide a thick oil which
  • customwas crystallized from ether/hexane
  • Quellen und Nachweise

    ORD-Eintrag
    ord-32be20121e2d469ca161d4426b0eacc4
    Quelldatensatz
    uspto-grants-1998_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05843968

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