Diethyl Ether → (R)-4-(1-Aminoethyl)cyclohexan-1-ol

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).

1. additionwas added
2. concentrationThe reaction mixture was concentrated in vacuo
3. dissolutionThe crude mixture was dissolved in MeOH (25 mL)
4. additionMP-Carbonate was added (11.75 g, 36.90 mmol)
5. filtrationThe resin was filtered
6. concentrationthe mother liquors were concentrated to dryness

ORD-Eintrag

ord-d538913161dc40ffb314b6ed97422ff5

Quelldatensatz

uspto-grants-2012_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08247421B2