Sulfuric Acid → 90103-48-3

HRID 485039

Reaktionsgleichung

Reaktionsgleichung von HRID 485039
[CH3:1][C:2]1([CH3:27])[C:10]2[CH:9]=[C:8]([C:11]([CH3:24])=[CH:12][C:13]3[CH:23]=[CH:22][C:16]([C:17]([O:19]CC)=[O:18])=[CH:15][CH:14]=3)[S:7][C:6]=2[C:5]([CH3:26])([CH3:25])[CH2:4][CH2:3]1.[OH-].[K+].S(=O)(=O)(O)O>C(O)C.O>[CH3:1][C:2]1([CH3:27])[C:10]2[CH:9]=[C:8](/[C:11](/[CH3:24])=[CH:12]/[C:13]3[CH:14]=[CH:15][C:16]([C:17]([OH:19])=[O:18])=[CH:22][CH:23]=3)[S:7][C:6]=2[C:5]([CH3:26])([CH3:25])[CH2:4][CH2:3]1

Komponenten

6

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

3.0 g of ethyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]benzoate are dissolved in 100 ml of ethanol and the solution is treated with a solution of 3.9 g of potassium hydroxide in 20 ml of water. After stirring at 50° C. for 3 hours, the mixture is cooled, poured into ice-water and acidified with 2N sulphuric acid. The mixture is extracted with ethyl acetate, the organic phase is washed with water, dried over sodium sulphate and evaporated. After recrystallization of the residue from ethyl acetate, there are obtained 2.4 g of p-[(E)-2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]benzoic acid in the form of pale yellowish crystals, m.p. 236°-238° C.

Aufarbeitung

  1. temperaturethe mixture is cooled
  2. extractionThe mixture is extracted with ethyl acetate
  3. washthe organic phase is washed with water
  4. dry with materialdried over sodium sulphate
  5. customevaporated
  6. customAfter recrystallization of the residue from ethyl acetate, there

Quellen und Nachweise

ORD-Eintrag
ord-514bebffff4e4448829c50a4155ab95c
Quelldatensatz
uspto-grants-1985_08
Patentnummer
US04535086

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