Reaktion #445456

Reaktionsgleichung

(+) 6,7-dichloro-2-cyclopentyl-2,3-dihydro-5-hydroxy-2-methyl-1H-inden-1-one

ethyl 4-bromobutanoate

→

(+)[(6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-yl)-oxy]butanoic acid

Ausbeute 99.6%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionextracted with ether
2. 2
   Waschenwashed with water
3. 3
   Sonstigethe ether evaporated at reduced pressure
4. 4
   workup.DISSOLUTIONThe residual oil is dissolved in acetic acid (150 ml)
5. 5
   Temperatur5% hydrochloric acid (50 ml), heated at 95° C. for 21/2 hours
6. 6
   Temperaturcooled
7. 7
   workup.ADDITIONtreated with ie (50 g)

Vorschrift

A mixture of (+) 6,7-dichloro-2-cyclopentyl-2,3-dihydro-5-hydroxy-2-methyl-1H-inden-1-one (14.25 g, 0.046 mole) potassium carbonate (12.5 g, 0.09 mole) and ethyl 4-bromobutanoate (17.5 g, 0.08 mole) in DMF (150 ml) is stirred at 55° C. for 4 hours then poured into ice water and extracted with ether, washed with water and the ether evaporated at reduced pressure. The residual oil is dissolved in acetic acid (150 ml) and 5% hydrochloric acid (50 ml), heated at 95° C. for 21/2 hours, cooled and treated with ie (50 g) to give 17.65 g of (+)[(6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-yl)-oxy]butanoic acid which melts at 75°-77° C. [α]D25 (C=2, acetone)=+36.8°.

Quelle