HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → {1-Azabicyclo[3.3.1]nonan-5-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-azabicyclo[3.3.1]nonane-5-carboxylate | HCID 19887573 | — |
| Reactant | lithium aluminium hydride THF | HCID 68718528 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {1-Azabicyclo[3.3.1]nonan-5-yl}methanol | HCID 19795980 | 98% |
Reaction Steps
A solution of 1-azabicyclo[3.3.1]nonane-5-carboxylic acid ethyl ester (9.08 g, 46 mmol) in anhydrous tetrahydrofuran (25 mL) was added dropwise to a cooled (-10° C.) solution of 1.0N lithium aluminum hydride/tetrahydrofuran (50 mL, 50 mmol) in a 3-neck, 250-mL flask under nitrogen at a rate to keep the reaction temperature below, 5° C. The mixture was stirred for 15 minutes at room temperature, refluxed for 45 minutes, cooled (0° C.), and carefully treated dropwise with water (2 mL), 15% sodium hydroxide (2 mL), and water (6 mL). The suspension was filtered through Celite and the solid was washed with tetrahydrofuran. The filtrate was concentrated in vacuo to afford 6.99 g (98%) of colorless solid; mp 64.0°-65.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244907 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-724adf2a51f8489d97c3c818d08a607f |
| Source note | uspto-grants-1993_09 |