Diazomethane → Methyl 7-(2-oxocyclopentyl)heptanoate
Reaktionsgleichung
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][CH:3]1[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14].[N+](=[CH2:18])=[N-]>CCOCC>[CH3:18][O:14][C:13](=[O:15])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH:3]1[CH2:4][CH2:5][CH2:6][C:2]1=[O:1]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 2.14 g. portion of 7-(2-oxocyclopentyl)-heptanoic acid was dissolved in 20 ml. of anhydrous ether and cooled to 0° C. in an ice bath. The stirred solution was then treated with ethereal diazomethane in about 1 ml. portions to control gas evolution until the yellow color persisted and bubbling was slow. The excess reagent was then blown off with a stream of nitrogen and the solvent evaporated at the rotovap. The residual oily ester was dried in vacuo over phosphorous pentoxide.
Aufarbeitung
- custombubbling
- customthe solvent evaporated at the rotovap
- dry with materialThe residual oily ester was dried in vacuo over phosphorous pentoxide
Quellen und Nachweise
- ORD-Eintrag
- ord-3f7f559b05714d5a81aa4dcef06c6133
- Quelldatensatz
- uspto-grants-1987_09
- Patentnummer
- US04695647
Notizen zur Reaktion
Wird geladen…