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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667315Generated: November 3, 2026

Tetrahydrofuran → HCID 23093701, compound

https://huagongshe.com/reaction/1667315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 23093706HCID 23093706—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 23093701HCID 2309370199%

Reaction Steps

To a solution of 209 mg of tert-butyl 4-{(E)-2-[4-(butoxycarbonyl)-2,6-dimethylphenyl]vinyl}piperidine-1-carboxylate in 5 ml of ethanol, 1.5 ml of 1N aqueous sodium hydroxide solution was added, followed by stirring at ambient temperature for 3.5 hours. After 1 ml of tetrahydrofuran was added to the reaction mixture, the mixture was stirred at 50° C. overnight. The solvent was evaporated under reduced pressure, water and 1.6 ml of 1N hydrochloric acid were added thereto. The formed precipitates were collected by filtration and dried to give 179 mg of 4-{(E)-2-[1-(tert-butoxycarbonyl)piperidin-4-yl]vinyl}-3,5-dimethylbenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044206B2
Source datasetuspto-grants-2011_10
ORD IDord-31933cd66cdc4fe7b42e928310ac2f9c
Source noteuspto-grants-2011_10