HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389107Generated: October 31, 2026
Tetrahydrofuran → HCID 58243583, compound
https://huagongshe.com/reaction/389107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl isothiocyanate | HCID 10966 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Product | HCID 58243583 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377923B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-995a44d6bc3c470fad3e82960f2ac9bb |
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| Source note | uspto-grants-2013_02 |
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