HCID 19614017, Verbindung → 2,2-Dimethyl-3-ethoxycarbonyl-cyclopropane-1-carbonitrile

HRID 1155650Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1155650
[N+](=C1CCCCCCCC1C1CCCCCCCC1)=[N-].[CH2:21]([O:23][C:24]([CH2:26][C:27]([CH3:33])([CH3:32])[CH:28](Br)[C:29]#[N:30])=[O:25])[CH3:22]>O>[CH2:21]([O:23][C:24]([CH:26]1[C:27]([CH3:33])([CH3:32])[CH:28]1[C:29]#[N:30])=[O:25])[CH3:22]

Komponenten

4

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

14.8 g (0.12 mol) of diazobicyclononane were added dropwise to a solution of 24.8 g (0.1 mol) of 3-bromo-3-cyano-2,2-dimethyl-propane-1-carboxylic acid ethyl ester in 100 ml of alcohol at 20° C. The mixture was then warmed to 50°-60° C. for 3 hours and cooled to 20° C., and 200 ml of water were added to the reaction mixture. The mixture was extracted twice with 100 ml of methylene chloride each time. The combined methylene chloride extracts were washed twice with 50 ml of 5% strength hydrochloric acid each time and twice with 50 ml of water each time, dried over sodium sulphate and concentrated. The residue was fractionated. 12.5 g (75% of theory) of 2-cyano-3,3-dimethyl-cyclopropane-1-carboxylic acid ethyl ester were obtained in the form of a colorless oil of boiling point 62°-64° C./1 mm Hg.

Aufarbeitung

  1. temperatureThe mixture was then warmed to 50°-60° C. for 3 hours
  2. extractionThe mixture was extracted twice with 100 ml of methylene chloride each time
  3. washThe combined methylene chloride extracts were washed twice with 50 ml of 5% strength hydrochloric acid each time
  4. dry with materialtwice with 50 ml of water each time, dried over sodium sulphate
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-aec9b1469aa7409487788c688755cf55
Quelldatensatz
uspto-grants-1982_06
Patentnummer
US04332745

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