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Tert-Butylhydroquinone → tert-Butyl-1,4-benzoquinone

HRID 67152
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 67152
[C:1]([C:5]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:6]=1[OH:7])([CH3:4])([CH3:3])[CH3:2]>[O-2].[O-2].[Mn+4].C1(C)C=CC=CC=1>[C:1]([C:5]1[C:6](=[O:7])[CH:8]=[CH:9][C:10](=[O:12])[CH:11]=1)([CH3:4])([CH3:2])[CH3:3]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 16043Tert-Butylhydroquinone

Produkt 1

HCID 19211tert-Butyl-1,4-benzoquinoneAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418406HCID 178418406, VerbindungKatalysatorHCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

16.6 g (0.10 mol) of 2-tert-butylhydroquinone was placed in a 200 cc 3-neck flask. After adding 17.4 g (0.20 mol) of powdery manganese dioxide, 100 cc of toluene was added thereto, and the mixture was heated with stirring. The temperature was maintained at 70° C. for 3 hours. After cooling to room temperature, the manganese dioxide was removed by filtration by means of suction using Celite as a filter aid. Then the manganese dioxide was washed with 50 cc of toluene, and the toluene was evaporated to dryness, by which 2-tert-butyl-1,4-benzoquinone was obtained. The yield was 80% and the melting point was 48°-50° C.

Aufarbeitung

  1. additionwas added
  2. temperaturethe mixture was heated
  3. temperatureAfter cooling to room temperature
  4. customthe manganese dioxide was removed by filtration by means of suction
  5. washThen the manganese dioxide was washed with 50 cc of toluene
  6. customthe toluene was evaporated to dryness, by which 2-tert-butyl-1,4-benzoquinone
  7. customwas obtained

Quellen und Nachweise

ORD-Eintrag
ord-5837863e67dc4d6886cf275d938e21dc
Quelldatensatz
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04345016

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