Réaction #1269869
ord-846643860ba44fb9b03aab34c35e7fd8
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Température
115°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe reaction was quenched with water (10 mL)
- 2ExtractionThe aqueous layer was extracted with EtOAc (3×10 mL)
- 3SéchageThe combined organic phase was dried over MgSO4
- 4Concentrationconcentrated
- 5Autreto give a residue which
- 6Autrewas purified by silica gel chromatography
Mode opératoire
Et3N (0.5 mL) was added into a solution of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (0.2 g) and benzoyl chloride (0.1 mL) in THF (10 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (10 mL). The aqueous layer was extracted with EtOAc (3×10 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 7-benzoyl-2,7-diazaspiro[4.4]nonane-2-carboxylate.