Pyridine → 1,1,1-Trifluoropropan-2-yl carbonochloridate

HRID 1518426

Reaktionsgleichung

Reaktionsgleichung von HRID 1518426
[F:1][C:2]([F:7])([F:6])[CH:3]([OH:5])[CH3:4].[Cl:8][C:9](Cl)([O:11]C(=O)OC(Cl)(Cl)Cl)Cl.N1C=CC=CC=1>C(OCC)C>[Cl:8][C:9]([O:5][CH:3]([CH3:4])[C:2]([F:7])([F:6])[F:1])=[O:11]

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a mixture of 1,1,1-trifluoro-2-propanol (114.1 mg, 10 mmol, Matrix Scientific) and triphosgene (98 mg, 0.33 mmol, Aldrich) in ethyl ether (10 mL) at −40° C. was added pyridine (80 μL, 1.0 mmol, EMD) in ethyl ether (1.0 mL) dropwise. The reaction mixture was warmed to 0° C. and stirred for 6 h. The flask containing the above reaction mixture was put into a refrigerator overnight and then filtered. The filtrate was concentrated in vacuo in ice both to colorless oil which was used directly in the next step.

Aufarbeitung

  1. additionThe flask containing the above reaction mixture
  2. customwas put into a refrigerator overnight
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated in vacuo in ice both to colorless oil which

Quellen und Nachweise

ORD-Eintrag
ord-3863166ae333446ea655f4b72feb6f7e
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08232404B2

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