1-Bromo-2-Chloroethane → HCID 86741981, Verbindung

HRID 2414077Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2414077
C([Li])CCC.C(NCC)C.[CH2:11]([CH:14]([CH2:17][CH2:18][CH3:19])[C:15]#[N:16])[CH2:12][CH3:13].Br[CH2:21][CH2:22][Cl:23]>CCCCCC.CCOCC.O>[Cl:23][CH2:22][CH2:21][C:14]([CH2:17][CH2:18][CH3:19])([CH2:11][CH2:12][CH3:13])[C:15]#[N:16]

Komponenten

8

Versuchsvorschrift

To the solution (245 ml) of 1,6M n butyllithium in hexane is added, drop by drop in an atmosphere of nitrogen and with stirring, the solution of 28.8 g of diethylamine in 100 ml of anhydrous ether. After 1 hour, the solution of 49.2 g of 2-propyl pentane nitrile in 100 ml of anhydrous ether is added at ambient temperature then, after return to ambient temperature, the solution of 49.1 g of 1-bromo 2-chloro ethane in 700 ml of anhydrous ether is added. The mixture is taken to reflux for 15 hours then, whilst cooling the reaction mixture in an ice bath, water is added. The organic phase is separated, washed with water, then with a dilute solution of hydrochloric acid and again with water. It is dried over sodium sulfate and the solvent is evaporated. The residue is distilled and a liquid is obtained; b.p./20 mm Hg: 140°-150° C.

Aufarbeitung

  1. temperatureto reflux for 15 hours
  2. temperaturewhilst cooling the reaction mixture in an ice bath
  3. customThe organic phase is separated
  4. washwashed with water
  5. dry with materialIt is dried over sodium sulfate
  6. customthe solvent is evaporated
  7. distillationThe residue is distilled
  8. customa liquid is obtained
  9. custom140°-150° C.

Quellen und Nachweise

ORD-Eintrag
ord-c1dc846746ee4ceabfa96141e679cd84
Quelldatensatz
uspto-grants-1988_01
Patentnummer
US04721710

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