Réaction #2275689

ord-05fd75c36a91493a884f71a1cc5e5ef4

Équation de réaction

CCN(CC)CC
Triethylamine
Cl.NC(CO)(CO)CO
Tris hydrochloride
COC(C)(C)OC
2,2-dimethoxypropane
Cc1ccc(S(=O)(=O)O)cc1
para-toluenesulfonic acid
CC1(C)OCC(N)(CO)CO1
product
Rendement 85.0%
CC1(C)OCC(N)(CO)CO1
(5-Amino-2,2-dimethyl-[1,3]dioxan-5-yl)-methanol
Rendement 85.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreresulted
  2. 2
    Autresolvent evaporated
  3. 3
    workup.DISSOLUTIONThe viscous crude was dissolved in triethylamine (40 ml)
  4. 4
    workup.ADDITIONethyl acetate (750 ml) added
  5. 5
    Filtrationthe white precipitate of ammonium salts was filtered off
  6. 6
    workup.STIRRINGafter stirring for 30 mins
  7. 7
    AutreThe filtrate was evaporated

Mode opératoire

Tris hydrochloride (51 g, 324 mmol) was suspended in dry DMF (100 ml) and 2,2-dimethoxypropane (39 g, 374 mmol) was added followed by para-toluenesulfonic acid (2.6 g, 13.5 mmol). The mixture was stirred in a sealed flask for 18 h at ambient temperature when a clear solution resulted. Triethylamine (2.5 ml) was added and solvent evaporated. The viscous crude was dissolved in triethylamine (40 ml) and ethyl acetate (750 ml) added and the white precipitate of ammonium salts was filtered off after stirring for 30 mins. The filtrate was evaporated to give the product as a colourless liquid in approx. 85% yield.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08323619B2uspto-grants-2012_12