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Resorcinol → 3,5-Di-tert-butyl-2',4,4'-trihydroxybenzophenone

HRID 1885510
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1885510
[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8](Cl)=[O:9])([CH3:4])([CH3:3])[CH3:2].[C:19]1([CH:26]=[CH:25][CH:24]=[C:22]([OH:23])[CH:21]=1)[OH:20].[Cl-].[Al+3].[Cl-].[Cl-]>[N+](C1C=CC=CC=1)([O-])=O>[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8]([C:24]1[CH:25]=[CH:26][C:19]([OH:20])=[CH:21][C:22]=1[OH:23])=[O:9])([CH3:4])([CH3:3])[CH3:2]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 5054ResorcinolHCID 37871873,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 197339413,5-Di-tert-butyl-2',4,4'-trihydroxybenzophenoneAusbeute 90,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7416NitrobenzeneLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

107.5 g of 3,5-di-tert-butyl-4-hydroxybenzoyl chloride and 48.4 g of resorcinol are suspended in 400 ml of nitrobenzene and warmed to 50° C. The brown solution is cooled to 0° C. 58.7 g of aluminium chloride are added in portions over the course of 45 minutes with vigorous stirring. The reaction mixture is slowly warmed to 20° C. over the course of 18 hours. The mixture is subsequently stirred at 50° C. for a further 4 hours, then cooled to room temperature and poured into 500 ml of hydrochloric acid/ice. The thick yellow suspension is extracted with ether, the ether phase is extracted with 500 ml of sodium hydroxide (15%), and the basic solution is washed three times with 250 ml of ether in each case, acidified to a pH of 1-2 using 15% hydrochloric acid and extracted with ether. The ether extracts are combined, dried and evaporated under reduced pressure, giving 124.4 g of 3,5-di-tert-butyl-2',4,4'-trihydroxybenzophenone, which, after recrystallisation from methanol, has a melting point of 192°-193° C.

Aufarbeitung

  1. temperatureThe brown solution is cooled to 0° C
  2. temperatureThe reaction mixture is slowly warmed to 20° C. over the course of 18 hours
  3. temperaturecooled to room temperature
  4. extractionThe thick yellow suspension is extracted with ether
  5. extractionthe ether phase is extracted with 500 ml of sodium hydroxide (15%)
  6. washthe basic solution is washed three times with 250 ml of ether in each case
  7. extractionextracted with ether
  8. customdried
  9. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-469c605f0ab34c91b6ad2b40fff676c0
Quelldatensatz
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05145766

Notizen zur Reaktion

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