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Hydroquinone → 4-(3-Bromopropoxy)phenol

HRID 839667
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 839667
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].[Br:9][CH2:10][CH2:11][CH2:12]Br.C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[Br:9][CH2:10][CH2:11][CH2:12][O:2][C:1]1[CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 785HydroquinoneHCID 80011,3-DibromopropaneHCID 11430Potassium Carbonate

Produkt 1

HCID 124399004-(3-Bromopropoxy)phenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6569Methyl Ethyl KetoneLösungsmittel

Versuchsvorschrift

A mixture of 88.0 g. (0.80 m.) of hydroquinone, 161.6 g. (0.80 m.) of 1,3-dibromopropane and 55.2 g. (0.40 m.) of potassium carbonate in 2 liters of 2-butanone was heated at reflux for 24 hours. The reaction mixture was filtered and the filtrate concentrated in vacuo. The solid and liquid phases of the residue were separated, and the liquid fraction was chromatographed on silica gel using chloroform-acetonitrile (95:5) as the eluant. There was thus obtained 37.2 g. of 4-(3-bromopropyloxy)phenol as a light brown oil which was used directly in the next reaction.

Aufarbeitung

  1. additionA mixture of 88.0 g
  2. temperatureat reflux for 24 hours
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate concentrated in vacuo
  5. customThe solid and liquid phases of the residue were separated
  6. customthe liquid fraction was chromatographed on silica gel
  7. customof 4-(3-bromopropyloxy)phenol as a light brown oil which was used directly in the next reaction

Quellen und Nachweise

ORD-Eintrag
ord-23bd87595a53454f8e2b7128ace45f69
Quelldatensatz
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04096280

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