Réaction #5737
ord-fdacc60898794503bab31670ff34e1da
Équation de réaction
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
40°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.ADDITIONpoured on to ice
- 2Autredecanted
- 3LavageThe organic phase was washed with water
- 4Autredried on sodium sulfate
- 5Autreevaporated to dryness under reduced pressure
Mode opératoire
30 mg of p-toluene sulfonic acid were added at 40° C. to a solution of 1 g of the product of Step B and 10 ml of methylene chloride and the reaction mixture was heated for 5 hours at 40° C., then poured on to ice, and decanted. The organic phase was washed with water, dried on sodium sulfate and evaporated to dryness under reduced pressure to obtain 860 mg of [1R-[1α-,3α-(RS*,RS*)]] 2,2-dimethyl-3-[2-trifluoromethyl-2-bromo-2-chloro-1-methylsulfonylethyl]-cyclopropane carboxylic acid melting at 138° C.