Water → 8-Azabicyclo[3.2.1]octane hydrochloride

HRID 2386955Notes

Reaction equation

HRID 2386955 reaction equation
[C@@H:1]12[N:8](C)[C@@H:5]([CH2:6][CH2:7]1)[CH2:4][CH2:3][CH2:2]2.C(=O)([O-])OCC[Cl:14].O>C1(C)C=CC=CC=1>[ClH:14].[CH:5]12[NH:8][CH:1]([CH2:7][CH2:6]1)[CH2:2][CH2:3][CH2:4]2

Participants

5

Conditions

Temperature
80 °C

Procedure

Tropane (1.0 mL, 7.44 mmol) was dissolved in toluene (10 mL), chloroethyl carbonate (2.2 mL, 23 mmol) was added slowly, and the mixture stirred at 80° C. for 24 hours. Distilled water was added to the reaction mixture, and the mixture extracted with ethyl acetate. The organic phase was dried and concentrated by anhydrous magnesium sulfate. The obtained oily residue was dissolved in concentrated hydrochloric acid (10 mL), and heated with stirring at 100° C. for 2 hours. The solvent was distilled off under reduced pressure, toluene was added to the residue, and the mixture distilled under reduced pressure to obtain the target substance (820 mg, 72%) as a colorless solid.

Workup

  1. extractionthe mixture extracted with ethyl acetate
  2. customThe organic phase was dried
  3. concentrationconcentrated by anhydrous magnesium sulfate
  4. dissolutionThe obtained oily residue was dissolved in concentrated hydrochloric acid (10 mL)
  5. temperatureheated
  6. stirringwith stirring at 100° C. for 2 hours
  7. distillationThe solvent was distilled off under reduced pressure, toluene
  8. additionwas added to the residue
  9. distillationthe mixture distilled under reduced pressure
  10. customto obtain the target substance (820 mg, 72%) as a colorless solid

Sources & evidence

ORD record
ord-d33019a9c6b74801bdd28b7c610ea2b6
Source dataset
uspto-grants-2012_09
Patent number
US08268842B2

Reaction notes

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