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 1N hydrochloric acid, and then 1N 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 | US04131611 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-e80dc43894ef4c9388b5e16f5e5316f6 |
| Source note | uspto-grants-1978_12 |