Methanol → HCID 54520137, Verbindung

HRID 1415327Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1415327
[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]3[CH:13]=[C:12]([C:14]([OH:16])=[O:15])[C:11]=3[CH:17]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.O.[CH3:19]O>S(=O)(=O)(O)O>[CH3:19][O:15][C:14]([C:12]1[C:11]2[CH:17]=[C:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)[CH:8]=[CH:9][C:10]=2[CH:13]=1)=[O:16]

Komponenten

5

Versuchsvorschrift

A solution of 15 g of 5-cyclohexyl-1-benzocyclobutenecarboxylic acid in 150 ml of absolute methanol and 1.5 ml of concentrated sulphuric acid is boiled for 14 hours under reflux whilst excluding water. The reaction mixture is evaporated in vacuo at 30° C to a volume of approx. 30 ml and the evaporation residue is partitioned between three times 200 ml of ether and twice 200 ml of ice water. The combined organic phases are successively washed with saturated sodium bicarbonate solution and water, dried over sodium sulphate and evaporated in vacuo. Distillation of the evaporation residue in a high vacuum yields 5-cyclohexyl-1-benzocyclobutenecarboxylic acid methyl ester in the fraction boiling at approx. 150° C/0.07 mm Hg.

Aufarbeitung

  1. temperatureunder reflux
  2. customThe reaction mixture is evaporated in vacuo at 30° C to a volume of approx. 30 ml
  3. customthe evaporation residue is partitioned between three times 200 ml of ether and twice 200 ml of ice water
  4. washThe combined organic phases are successively washed with saturated sodium bicarbonate solution and water
  5. dry with materialdried over sodium sulphate
  6. customevaporated in vacuo
  7. distillationDistillation of the evaporation residue in a high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-e0e306aef69a46398f4565672622381d
Quelldatensatz
uspto-grants-1977_01
Patentnummer
US04004026

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