Methanol → 3(2,2-Dichlorovinyloxy)benzyl alcohol

HRID 1576231

Reaktionsgleichung

Reaktionsgleichung von HRID 1576231
[Cl:1][C:2]([Cl:13])=[CH:3][O:4][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH2:8]Br.C1(C)C=CC(S([O-])(=O)=[O:21])=CC=1.[Na+].CO.O>C1(C)C=CC=CC=1>[Cl:1][C:2]([Cl:13])=[CH:3][O:4][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH2:8][OH:21]

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A mixture 3(2,2-dichlorovinyloxy)benzyl bromide (2.8 g), sodium p-toluene sulphonate (2.0 g) and methanol (20 ml) is warmed to 50°C for 1 hour, after which water (20 ml) and toluene (20 ml) is added with agitation. The toluene layer is separated, washed with water and concentrated by evaporation of the solvent under reduced pressure. The concentrate is then added dropwise to a 15% (w/v) aqueous solution of potassium hydroxide (100 ml) and the mixture warmed to 60°C for 1 hour, cooled to the ambient temperature and extracted with a mixture of toluene (10 ml) and methyl iso-butylketone (10 ml), the extracts dried over anhydrous magnesium sulphate and the solvents evaporated under reduced pressure to yield 3(2,2-dichlorovinyloxy)benzyl alcohol as a residual pale yellow oil.

Aufarbeitung

  1. customThe toluene layer is separated
  2. washwashed with water
  3. concentrationconcentrated by evaporation of the solvent under reduced pressure
  4. additionThe concentrate is then added dropwise to a 15% (w/v) aqueous solution of potassium hydroxide (100 ml)
  5. temperaturecooled to the ambient temperature
  6. extractionextracted with a mixture of toluene (10 ml) and methyl iso-butylketone (10 ml)
  7. dry with materialthe extracts dried over anhydrous magnesium sulphate
  8. customthe solvents evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b971276c258d47b8a9598a4d28b968ea
Quelldatensatz
uspto-grants-1976_09
Patentnummer
US03979519

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