tert-Butanol → 4-tert-Butyl-3-chlorophenol

HRID 1165443

Reaktionsgleichung

Reaktionsgleichung von HRID 1165443
[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[CH3:9][C:10](O)([CH3:12])[CH3:11]>CCCCCC.P(=O)(O)(O)O>[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][C:7]=1[C:10]([CH3:12])([CH3:11])[CH3:9]

Komponenten

5

Edukt 2

HCID 6386tert-ButanolHCID 79333-Chlorophenol

Produkt 1

HCID 134994724-tert-Butyl-3-chlorophenolAusbeute 0,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1004Phosphoric AcidLösungsmittelHCID 8058HexaneLösungsmittel2×

Versuchsvorschrift

A mixture of 50 g (0.39 mol) of 3-chlorophenol in 250 ml of hexane and 125 ml of 85% phosphoric acid was heated to reflux. A solution of 43.2 g (0.584 mol) of 2-methyl-2-propanol in 25 ml of hexane was added over 1.5 hours. After addition, the reaction mixture was refluxed for 4 hours. The organic phase was separated and extracted four times with 30 ml of lN sodium hydroxide solution. The combined aqueous fractions were made acidic and extracted with methylene chloride. The organic phase was dried and evaporated at 90° C. (25 mm). The residue was crystallized from hexane. There was obtained 0.46 g (2.49 mmol, 0.6%) of 3-chloro-4-(1,1-dimethylethyl)phenol as a white solid after crystallization from hexane; mp 65°-67° C.

Aufarbeitung

  1. temperaturewas heated to reflux
  2. additionAfter addition
  3. temperaturethe reaction mixture was refluxed for 4 hours
  4. customThe organic phase was separated
  5. extractionextracted four times with 30 ml of lN sodium hydroxide solution
  6. extractionextracted with methylene chloride
  7. customThe organic phase was dried
  8. customevaporated at 90° C. (25 mm)
  9. customThe residue was crystallized from hexane

Quellen und Nachweise

ORD-Eintrag
ord-807a84e578c14241bdcb3dfe71f4655f
Quelldatensatz
uspto-grants-1990_03
Patentnummer
US04910202

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