HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14443Generated: October 26, 2026
Hydrochloric Acid → 9-Methyl-3-oxa-9-azatricyclo(3.3.1.02,4)nonan-7-ol
https://huagongshe.com/reaction/14443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178481191 | HCID 178481191 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 9-Methyl-3-oxa-9-azatricyclo(3.3.1.02,4)nonan-7-ol | HCID 274439 | 50% |
Reaction Steps
Sodium borohydride (39.0 g, 1.03 mol) was added portionwise to a stirred suspension of scopolamine (75 g, 171 mmol) in ethanol (743 mL), at 0° C. under a nitrogen atmosphere and the reaction mixture was stirred at ambient temperature for 24 h. The mixture was then acidified with 2M hydrochloric acid in diethyl ether (600 mL) and stirred for another 24 h at ambient temperature. The reaction mixture was filtered and the resulting solid was washed with diethyl ether. The dried solid was dissolved in the minimum amount of 10% aqueous potassium carbonate solution and extracted with trichloromethane (6×150 mL). The combined organic extracts were dried (magnesium sulfate), filtered and the solvent was removed under reduced pressure to give the title compound as crystals (13.2 g, 85.5 mmol, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07732441B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-39214d042e754036b9a6f6c7890a5e32 |
|---|
| Source note | uspto-grants-2010_06 |
|---|