HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → {1-Azabicyclo[3.2.1]octan-5-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-azabicyclo[3.2.1]octane-5-carboxylate | HCID 15663615 | — |
| Reactant | lithium aluminium hydride THF | HCID 68718528 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {1-Azabicyclo[3.2.1]octan-5-yl}methanol | HCID 19795992 | — |
Reaction Steps
A cooled (0° C.) solution of 1.0N lithium aluminum hydride/tetrahydrofuran (55 mL, 55 mmol) under nitrogen was treated dropwise with a solution of 1-azabicyclo[3.2.1]octane-5-carboxylic acid ethyl ester (9.17 g, 50 mmol) in anhydrous tetrahydrofuran (20 mL), stirred for 30 minutes at room temperature, refluxed for one hour, and cooled (0° C.). In sequence, water (2.1 mL), 15% sodium hydroxide solution (2.1 mL) and water (6.3 mL) were carefully added dropwise, and the mixture was filtered through Celite (the solid was washed with tetrahydrofuran) and concentrated in vacuo to afford 6.50 g (92%) of viscous, colorless oil, which can be used as is or can be solidified on cooling; mp 44°-47° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244907 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-3f6f7292f4214dacbbc44e42e9963d38 |
| Source note | uspto-grants-1993_09 |