HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Methyl-1-(p-tolyl)-3-azabicyclo[3.1.0]hexane hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(p-Tolyl)-3-azabicyclo[3.1.0]hexan-2-one | HCID 12891385 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl-1-(p-tolyl)-3-azabicyclo[3.1.0]hexane hydrochloride | HCID 23332366 | — |
Reaction Steps
Using the method of M. Takeda, et al., Chem. Pharm. Bull., 24, 2312 (1976), 1-(p-tolyl)-3-azabicyclo[3.1.0]hexan-2-one is reacted with methyllithium followed by sodium borohydride. Excess reagents are decomposed with methanol, followed by 1 N hydrochloric acid, and then 1 N sodium hydroxide and then evaporation of the solution gives a residue which is dissolved in ether. This solution is dried over sodium sulfate and filtered, and to the filtrate is added dry hydrogen chloride. Filtration of this suspension gives 2-methyl-1-(p-tolyl)-3-azabicyclo[3.1.0]hexane hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04196120 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-31ac89073c614fa1a877f8f75afc8f43 |
| Source note | uspto-grants-1980_04 |