HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 19976914, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 19976965 | HCID 19976965 | — |
| Product | HCID 19976914 | HCID 19976914 | — |
Reaction Steps
Pyrrolidine (5 ml) was added to 0.98 g (3.9 mmol) of 3-phenyl-5-(1-cyclohexenoyl)isoxazole prepared above in the procedure (1). The resultant mixture was stirred at room temperature for 1 hour and then concentrated under reduced pressure. To the concentrate was added diethyl ether and then 10% hydrochloric acid, whereby the reaction product was extracted in a water layer. The water layer was collected, alkalinized with a 10% aqueous solution of sodium hydroxide, and then extracted with dichloromethane. methane. The solvent was distilled off, so that 3-phenyl-5-{2-(1-pyrrolidinyl)cyclohexanoyl} isoxazole was obtained as yellow crystals. Analytical results of the crystals obtained: Yield: 0.44 g (35%). Melting point: 109°-111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05338857 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-c8e2c0b648f3432684ba1ace56cccf3a |
| Source note | uspto-grants-1994_08 |