Reacción #1929067

ord-71dd19b43fab4d769598e49585922ce2

Ecuación de reacción

NC1(C(=O)O)CCC(F)(F)CC1
compound
NC1(C(=O)O)CCC(F)(F)CC1
1-Amino-4,4-difluorocyclohexanecarboxylic acid
CO
methanol
O=S(Cl)Cl
thionyl chloride
COC(=O)C1(N)CCC(F)(F)CC1.Cl
Methyl 1-amino-4,4-difluorocyclohexanecarboxylate hydrochloride

Condiciones de reacción

Temperatura
70°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was then cooled to 5° C.
  2. 2
    Filtraciónthe precipitate was filtered off with suction
  3. 3
    ConcentraciónThe solution was concentrated
  4. 4
    Otroa rotary evaporator
  5. 5
    Otrothe residue was crystallized

Procedimiento

Under argon, 4.30 g of the compound from Example 3A were initially charged in 100 ml of methanol at 0 to 5° C. 10 ml of thionyl chloride were added dropwise, and the mixture was stirred at 0° C. for 30 minutes and at 70° C. for 24 h. The mixture was then cooled to 5° C. and the precipitate was filtered off with suction. The solution was concentrated using a rotary evaporator and the residue was crystallized using methyl tert-butyl ether. This gave 5.20 g (quantitative, still contains salts) of the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08946124B2uspto-grants-2015_02