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Diethyl octylmalonate → 2-Octylpropane-1,3-diol

HRID 2050135
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2050135
C([O:3][C:4](=O)[CH:5]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:6](OCC)=[O:7])C>Cl>[CH2:11]([CH:5]([CH2:4][OH:3])[CH2:6][OH:7])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 252340Diethyl octylmalonate

Produkt 1

HCID 3160622-Octylpropane-1,3-diolAusbeute 41 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

Borane methyl sulfide (BMS) complex (80 g, 1 m) was added dropwise to a mixture of diethyl-n-octylmalonate (90 g, 0.33) and tolune (400 ml) with stirring at room temperature. Stirring was continued for an additional hour. The mixture was refluxed gently for 10 hours, cooled to 20° C., and then poured slowly into ice-cold methanol (400 ml) with stirring and left to stand overnight. The solvent was stripped off and the residue was stirred with 10% hydrochloric acid solution (400 ml) overnight. The resulting mixture was extracted with chloroform (2×70 ml) and washed with water until neutral to litmus. The solvent was evaporated and the residue was vacuum distilled to yield 2-n-octylpropane-1,3-diol (25.5 g, 41%) bp 135°-140° C./0.5-0.8 mm.

Aufarbeitung

  1. stirringStirring
  2. waitwas continued for an additional hour
  3. temperatureThe mixture was refluxed gently for 10 hours
  4. temperaturecooled to 20° C.
  5. stirringwith stirring
  6. waitleft
  7. extractionThe resulting mixture was extracted with chloroform (2×70 ml)
  8. washwashed with water until neutral to litmus
  9. customThe solvent was evaporated
  10. distillationdistilled

Quellen und Nachweise

ORD-Eintrag
ord-164aeeb371254c0ab6bf951732053e6a
Quelldatensatz
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04200580

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