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Water → (3-Methoxy-4-methylphenyl)methanol

HRID 745245
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 745245
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[CH3:12])[C:6](O)=[O:7].O>O1CCCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[CH3:12])[CH2:6][OH:7]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 962WaterHCID 815794-Methyl-m-anisic acid

Produkt 1

HCID 11744818(3-Methoxy-4-methylphenyl)methanolAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Into a solution of 10.0 g of 3-methoxy-4-methylbenzoic acid in 100 ml of dried tetrahydrofuran, while being cooled in ice and stirred under a nitrogen stream, was added dropwise over a period of 15 minutes 80 ml of a 1M solution of borane-tetrahydrofuran complex in tetrahydrofuran. The mixture was then stirred at room temperature for 3 hours. After addition of 10 ml of water, the reaction mixture was stripped of the solvent by distillation. The residue was dissolved in ether, washed with saturated aquecus sodium bicarbonate solution, then with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and stripped of the solvent by distillation to yield 7.6 g of 3-methoxy-4-methylbenzyl alcohol in the form of yellow oil.

Aufarbeitung

  1. stirringThe mixture was then stirred at room temperature for 3 hours
  2. distillationthe reaction mixture was stripped of the solvent by distillation
  3. dissolutionThe residue was dissolved in ether
  4. washwashed with saturated aquecus sodium bicarbonate solution
  5. dry with materialwith saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  6. distillationstripped of the solvent by distillation

Quellen und Nachweise

ORD-Eintrag
ord-cba8e561ae12412a93e0ec96a972bd30
Quelldatensatz
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04598077

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