Réaction #6668

ord-c7929215a1044905b53af2ac9d1a111e

Équation de réaction

O=C(OC(F)(F)C(F)(OC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F)C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F
CF3(CF2)9OCF(CF3)CF2OCOCF(CF3)OCF2CF2CF3
[F-].[Na+]
NaF
O=C(F)C(F)(OC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F
CF3(CF2)9OCF(CF3)COF
Rendement 63.8%

Conditions de réaction

Température
150°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreadjusted to a temperature of 20° C.
  2. 2
    TempératureAfter cooling
  3. 3
    Autrethe liquid sample (1.9 g) was recovered

Mode opératoire

CF3(CF2)9OCF(CF3)CF2OCOCF(CF3)OCF2CF2CF3 (2.0 g) obtained in Example 23 was charged into a flask together with a NaF powder (0.05 g) and heated at 150° C. for 24 hours in an oil bath with vigorous stirring. At an upper part of the flask, a reflux condenser adjusted to a temperature of 20° C., was installed. After cooling, the liquid sample (1.9 g) was recovered. By GC-MS, it was confirmed that CF3CF(OCF2CF2CF3)COF and the above-identified compound were the main products. The yield was 63.8%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07083705B2uspto-grants-2006_08