HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (+/-)3-(4-Chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene Malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | 3-(4-Chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-ol | HCID 434488 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+/-)3-(4-Chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene Malonate | HCID 18694314 | — |
Reaction Steps
The title compound was prepared from 3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-ol (4 g, 16 mmol), glacial acetic acid (15 mL) and concentrated hydrochloric acid (15 mL). Yield of free base (3.6 g, 97%). Some of the free base (1.44 g, 6 mmol) was dissolved in ethanol (96%) and added malonic acid (0.62 g, 6 mmol) in ethanol (96%). The resulting solution was concentrated to an oil, the oil was trituated in diethyl ether, the title compound precipitated as powder and was isolated by filtration. Yield (1.4 g, 71%) as white crystals m.p. 100.8-102.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100275 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-2fbe958019e241fa8796086258e6865d |
| Source note | uspto-grants-2000_08 |