Réaction #1435709

ord-92a6ac4c660741eba4d2140a5c81a379

Équation de réaction

O=S(=O)(O)O
Sulfuric acid
[H-].[Na+]
Sodium hydride
CC(=O)c1cccs1
2-Acetylthiophene
CCOC(=O)C(F)(F)C(F)(F)F
Ethyl pentafluoropropionate
O=C(CC(=O)C(F)(F)C(F)(F)F)c1cccs1
product
O=C(CC(=O)C(F)(F)C(F)(F)F)c1cccs1
4,4,5,5,5-Pentafluoro-1-(2-thienyl)-1,3-pentanedione

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.WAITthe stirring was continued overnight
  2. 2
    Autrethe phases were separated
  3. 3
    LavageThe organic phase was washed with water (50 ml) and it
  4. 4
    Autrewas evaporated to dryness
  5. 5
    workup.DISTILLATIONThe residue was distilled (b.p. 92–94° C./0.15 mbar)

Mode opératoire

2-Acetylthiophene (4.3 ml) was dissolved in dry toluene (40 ml). Sodium hydride (60%, 3.2 g) was added slowly and the mixture was stirred for 15 minutes. Ethyl pentafluoropropionate (13.44 g) was added and the stirring was continued overnight. Sulfuric acid (10%, 50 ml) was added and the phases were separated. The organic phase was washed with water (50 ml) and it was evaporated to dryness. The residue was distilled (b.p. 92–94° C./0.15 mbar) to give the product (9.0 g). 1H NMR (CDCl3): 6.50 (s, 1 H); 7.21 (dd, 1 H, J=3.9 & 4.9); 7.77 (dd, 1 H, J=1.1 & 4.9 Hz); 7.85 (dd, 1 H, J=1.1 & 3.9 Hz). IR (film): 1592 (C═O); 1202 (C—F).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07211440B2uspto-grants-2007_05