Réaction #69116

Équation de réaction

Tert-butyl (R)-1-(4-hydroxycyclohexyl)ethylcarbamate

Ether

→

title compound

(R)-4-(1-aminoethyl)cyclohexanol

Solvants

dichloromethane

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONwas added
2. 2
   ConcentrationThe reaction mixture was concentrated in vacuo
3. 3
   workup.DISSOLUTIONThe crude mixture was dissolved in MeOH (25 mL)
4. 4
   workup.ADDITIONMP-Carbonate was added (11.75 g, 36.90 mmol)
5. 5
   FiltrationThe resin was filtered
6. 6
   Concentrationthe mother liquors were concentrated to dryness

Mode opératoire

Tert-butyl (R)-1-(4-hydroxycyclohexyl)ethylcarbamate (4.49 g, 18.45 mmol) was dissolved in dichloromethane (25 mL) and cooled to 0° C. under nitrogen. HCl 2M in Ether (27.68 mL of 2 M, 55.35 mmol) was added and the reaction allowed to warm slowly to ambient temperature for 18 hours. The reaction mixture was concentrated in vacuo. The crude mixture was dissolved in MeOH (25 mL). MP-Carbonate was added (11.75 g, 36.90 mmol) and the reaction mixture was stirred for 3 hours. The resin was filtered and the mother liquors were concentrated to dryness to afford the title compound as an off white solid (2.39 g, 90% yield).

Source