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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742542Generated: November 2, 2026

Pyrrolidine → HCID 19976914, compound

https://huagongshe.com/reaction/1742542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantHCID 19976965HCID 19976965—
ProductHCID 19976914HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338857
Source datasetuspto-grants-1994_08
ORD IDord-c8e2c0b648f3432684ba1ace56cccf3a
Source noteuspto-grants-1994_08