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Ethyl Bromide → 4-Acetyl-4'-ethoxybiphenyl

HRID 1608748
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1608748
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[CH2:17](Br)[CH3:18].C(=O)([O-])[O-].[K+].[K+].C1(=O)CCCCC1>>[CH2:17]([O:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1)[CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6332Ethyl BromideHCID 7967CyclohexanoneHCID 11430Potassium CarbonateHCID 103308064-(4-Acetylphenyl)phenol

Produkt 1

HCID 232504334-Acetyl-4'-ethoxybiphenyl

Versuchsvorschrift

A reaction vessel was charged with 230 g of 4-hydroxy-4'-acetylbiphenyl, 164 g of ethyl bromide, 276 g of potassium carbonate and 1.7 l of cyclohexanone. The mixture was reacted together under agitation for 3 hours at 65°-70° C. and then for 6 hours at 95°-100° C. The reaction liquid was filtered and the resultant solid matter was washed with benzene. The filtrate and the washing liquid were combined, washed with water and dried over Glauber's salt, The solvents were distilled off and the residue was recrystallized from a mixed solvent of acetone-methanol to obtain 4-ethoxy-4'-acetylbiphenyl.

Aufarbeitung

  1. customThe mixture was reacted together under agitation for 3 hours at 65°-70° C.
  2. customThe reaction liquid
  3. filtrationwas filtered
  4. washthe resultant solid matter was washed with benzene
  5. washwashed with water
  6. dry with materialdried over Glauber's salt
  7. distillationThe solvents were distilled off
  8. customthe residue was recrystallized from a mixed solvent of acetone-methanol

Quellen und Nachweise

ORD-Eintrag
ord-908052fa35794ecbae223747716a08f4
Quelldatensatz
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05397504

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