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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389107Generated: October 31, 2026

Tetrahydrofuran → HCID 58243583, compound

https://huagongshe.com/reaction/389107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl isothiocyanateHCID 10966—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ProductHCID 58243583HCID 58243583—

Reaction Steps

Ethyl isothiocyanate (0.60 ml) was added to a solution of ethyl piperidine-4-carboxylate (1.02 g) in THF (20 ml), followed by stirring at room temperature for one hour. The reaction solution was concentrated and the resulting colorless oily product was made into an ethanol solution (20 ml), iodomethane (2.0 ml) was added thereto, followed by stirring at 60° C. for 3 hours. The reaction solution was concentrated, an aqueous saturated sodium hydrogen carbonate solution was added thereto, followed by extraction with chloroform, the organic layer was washed with saturated brine and was dried over anhydrous magnesium sulfate, and the solvent was evaporated to obtain ethyl 1-[(ethylimino)(methylsulfanyl)methyl]piperidine-4-carboxylate (1.84 g) as a light yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-995a44d6bc3c470fad3e82960f2ac9bb
Source noteuspto-grants-2013_02