1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1) → 3-Quinuclidinone

HRID 1465988Notes

Reaction equation

HRID 1465988 reaction equation
Cl.[N:2]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[C:4](=[O:10])[CH2:3]2.C[O-].[Na+]>CO>[N:2]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[C:4](=[O:10])[CH2:3]2

Participants

4

Reactant 2

HCID 1020191-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 10942334Sodium Methoxide

Product 1

HCID 195073-Quinuclidinone

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

100 g (0.62 mol) of quinuclidin-3-one hydrochloride are suspended in 21 of methanol. At 0° C., a solution of 33.4 g (0.62 mol) of sodium methoxide in 250 ml of methanol is slowly added dropwise. The mixture is stirred at room temperature for 16 h. The resulting precipitate is filtered off with suction, and the filtrate is concentrated in vacuo. The residue is partitioned between chloroform and water and extracted with chloroform the combined organic phases are dried over sodium sulfate and concentrated in vacuo. 58.8 g (75.9% of theory) of the title compound are obtained.

Workup

  1. filtrationThe resulting precipitate is filtered off with suction
  2. concentrationthe filtrate is concentrated in vacuo
  3. customThe residue is partitioned between chloroform and water
  4. extractionextracted with chloroform the combined organic phases
  5. dry with materialare dried over sodium sulfate
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-0454c6120bde4e05869ad486b214e459
Source dataset
uspto-grants-2015_04
Patent number
US09000008B2

Reaction notes

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