Trifluoroacetonitrile → HCID 178472209, Verbindung

HRID 542128

Reaktionsgleichung

Reaktionsgleichung von HRID 542128
[C:1]([CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:4])[CH2:2][CH3:3].[Na].[F:12][C:13]([F:17])([F:16])[C:14]#[N:15]>COCCOC>[NH2:15]/[C:14](/[C:13]([F:17])([F:16])[F:12])=[C:5](/[C:1](=[O:4])[CH2:2][CH3:3])\[C:6]([O:8][CH2:9][CH3:10])=[O:7]

Komponenten

5

Versuchsvorschrift

To a mechanically stirred solution of 287 g (1.99 mol) of ethyl propionylacetate in 500 ml of dry DME was added under nitrogen 8.6 g (0.348 mol) of freshly cut sodium. After all sodium had dissolved, 256 g (2.69 mol) of trifluoroacetonitrile was added over a 35 hour period. The reaction mixture was concentrated. The residue was washed with water and extracted into 500 ml of ether. The ether solution was dried and concentrated. The residue was kugelrohr distilled at 67 Pa. and then was redistilled at 67 Pa through a spinning band column. The first fraction (bp 40°-78° C.) was discarded. The next fraction (bp 79°-82° C.) was 151 g (31.6%) of product, nD25 1.4574.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. washThe residue was washed with water
  3. extractionextracted into 500 ml of ether
  4. dry with materialThe ether solution was dried
  5. concentrationconcentrated
  6. distillationThe residue was kugelrohr distilled at 67 Pa
  7. distillationand then was redistilled at 67 Pa through a spinning band column

Quellen und Nachweise

ORD-Eintrag
ord-1252b550ae124bd5b158217c426e7714
Quelldatensatz
uspto-grants-1987_04
Patentnummer
US04655816

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