Reaktion #88529

Reaktionsgleichung

(1R,3S,4S)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid hydrogen chloride

lithium tetrahydroaluminate

→

(1R,3S,4S)-2-azabicyclo[2.2.1]heptan-3-ylmethanol

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction was quenched with a few drops of water
2. 2
   workup.ADDITIONdiluted with diethyl ether (50 mL) and tetrahydrofuran (25 mL)
3. 3
   workup.ADDITIONThe reaction mixture was basified to a pH of ˜11 by the addition of potassium hydroxide pellets
4. 4
   workup.STIRRINGstirred vigorously for 30 minutes
5. 5
   FiltrationThe reaction mixture was filtered over sodium sulfate
6. 6
   Einengenconcentrated in vacuo
7. 7
   workup.DISSOLUTIONredissolved in methylene chloride (10 mL)
8. 8
   Trocknendried once more over sodium sulfate
9. 9
   Filtrationfiltered
10. 10
    Einengenconcentrated in vacuo
11. 11
    Sonstigeto afford a yellow crystalline solid, which
12. 12
    Sonstigewas used in the next step without any further purification (400 mg, 100%)

Vorschrift

To a slurry of (1R,3S,4S)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid hydrogen chloride (500 mg, 3 mmol) in tetrahydrofuran (4.6 mL) was added lithium tetrahydroaluminate (1N solution in tetrahydrofuran, 5.7 mL, 6 mmol) dropwise over 10 minutes. The reaction mixture was stirred overnight at ambient temperature under an atmosphere of nitrogen. The reaction was quenched with a few drops of water, diluted with diethyl ether (50 mL) and tetrahydrofuran (25 mL). The reaction mixture was basified to a pH of ˜11 by the addition of potassium hydroxide pellets and then stirred vigorously for 30 minutes. The reaction mixture was filtered over sodium sulfate, concentrated in vacuo, redissolved in methylene chloride (10 mL), dried once more over sodium sulfate, filtered, and concentrated in vacuo to afford a yellow crystalline solid, which was used in the next step without any further purification (400 mg, 100%).

Quelle