Sulfuric Acid → 3-(3-Oxobut-1-enyl)-2,4,4-trimethylcyclohex-2-en-1-one

HRID 1446783

Reaktionsgleichung

[CH3:1][C:2]1[CH:7]([OH:8])[CH2:6][CH2:5][C:4]([CH3:10])([CH3:9])[C:3]=1[CH:11]=[CH:12][C:13](=[O:15])[CH3:14].O.O.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[Na+].[Na+].S(=O)(=O)(O)O>CCOCC>[CH3:1][C:2]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]([CH3:9])([CH3:10])[C:3]=1[CH:11]=[CH:12][C:13](=[O:15])[CH3:14]

Komponenten

Reaktionsbedingungen

Temperatur: 5 °C

Versuchsvorschrift

To a solution, pre-cooled to 0° C., of 140 g (0.068 mol) of 4-(2,6,6-trimethyl-3-hydroxy-cyclohex-1-en-1-yl)-but-3-en-2-one in 500 ml of ether are added dropwise over a period of 10 minutes 700 ml of an aqueous solution, cooled to 0° C., of 202.6 g of sodium dichromate dihydrate and 186 g of concentrated sulphuric acid with intensive cooling and good stirring so that a temperature of 5° C. is not exceeded. The mixture is then stirred for a further 5 minutes at 5° C., treated with 500 ml of ether, the ether phase is washed three times with water, three times with soda solution and again three times with water, dried over sodium sulphate and concentrated. Distillation of the resulting 125 g of crude product over a 10 cm Widmer column gave 103 g of more than 94% g of more than 94% pure 4-(2,6,6 -trimethyl-3-oxo-cyclohex-1-en-1-yl)-but-3-en-2-one of boiling point 109°-110° C./0.05 mm Hg; melting point 50°-51° C.

Aufarbeitung

temperaturewith intensive cooling
stirringThe mixture is then stirred for a further 5 minutes at 5° C.
washthe ether phase is washed three times with water, three times with soda solution and again three times with water
dry with materialdried over sodium sulphate
concentrationconcentrated
distillationDistillation of the resulting 125 g of crude product over a 10 cm Widmer column

Quellen und Nachweise

ORD-Eintrag: ord-35bc80ab15be4079989d30cb1481f97c
Quelldatensatz: uspto-grants-1982_02
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04313856

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