4-Phenethyloxybenzoic Acid Methyl Ester → (4-Phenethyloxyphenyl)methanol

HRID 1827965Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1827965
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:6][CH:5]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C(OCC)C>[CH2:11]([O:10][C:7]1[CH:6]=[CH:5][C:4]([CH2:3][OH:2])=[CH:9][CH:8]=1)[CH2:12][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Komponenten

4

Edukt 2

HCID 120638344-Phenethyloxybenzoic Acid Methyl EsterHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 12990905(4-Phenethyloxyphenyl)methanolAusbeute 98,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

4-Phenethyloxybenzoic acid methyl ester 10 (7.66 g, 29.89 mmol) was dissolved in diethyl ether and chilled to 0° C. LiAlH4 was slowly added and allowed to stir at 0° C. for 3 hours. The mixture was quenched with H2O. After addition of 3N NaOH the mixture was allowed to stir for 30 min. The mixture was then acidified with 4.5N HCl, extracted, dried, and concentrated in vacuo to give about 6.7g of a crystalline (4-phenethyloxyphenyl)methanol 11.

Aufarbeitung

  1. customThe mixture was quenched with H2O
  2. additionAfter addition of 3N NaOH the mixture
  3. stirringto stir for 30 min
  4. extractionextracted
  5. customdried
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-093d5a592e824bce8ebeba115df374af
Quelldatensatz
uspto-grants-2006_06
Patentnummer
US07056903B2

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