Réaction #2275686

ord-c5b88feed488451a88ad389579438ffc

Équation de réaction

OCCNCC(O)CO
N-(hydroxyethyl)-amino-2,3-propanediol
Cl
HCl
C1COCCO1
dioxane
COC(C)(C)OC
2,2-dimethoxypropane
CC1(C)OCC(CNCCO)O1
liquid
Rendement 100.0%
CC1(C)OCC(CNCCO)O1
2-[(2,2-Dimethyl-[1,3]-dioxolan-4-yl-methyl)-amino]-ethanol
Rendement 100.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvents removed by rotary evaporation
  2. 2
    workup.DISSOLUTIONThe viscous crude mixture was dissolved into triethylamine (30 mL) and ethyl acetate (500 mL)
  3. 3
    workup.STIRRINGstirred at RT for 30 min
  4. 4
    FiltrationThe mixture was filtered
  5. 5
    Lavagethe collected solid washed several times with ethyl acetate
  6. 6
    AutreThe filtrate was then evaporated on a high vacuum rotary evaporator at 40° C.

Mode opératoire

The N-(hydroxyethyl)-amino-2,3-propanediol (16.5 g, 122 mmol) was treated with a solution of HCl in dioxane (33.5 ml, 134 mmol). To this solution were added 2,2-dimethoxypropane (15.3 g, 147 mmol), DMAC (50 mL), and a catalytic amount of para-toluene sulphonic acid (0.006 mol, 1.16 g). The mixture stirred at room temperature for 24 hours. Triethylamine (1 mL) was then added, and the solvents removed by rotary evaporation. The viscous crude mixture was dissolved into triethylamine (30 mL) and ethyl acetate (500 mL) and stirred at RT for 30 min. The mixture was filtered and the collected solid washed several times with ethyl acetate. The filtrate was then evaporated on a high vacuum rotary evaporator at 40° C. to give a yellow liquid (0.122 mol, 99% yield).

Source

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