HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620473Generated: November 3, 2026
tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 86678665, compound
https://huagongshe.com/reaction/1620473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | 4-Sulfanylidene-1,3-thiazolidin-2-one | HCID 1539595 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86628739 | HCID 86628739 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86678665 | HCID 86678665 | 66.6% |
Reaction Steps
tert-Butyl 4-formylpiperidine-1-carboxylate (7.6 g) and 4-thioxo-1,3-thiazolidin-2-one (4.98 g) were suspended in ethanol (200 mL), potassium tert-butoxide (4.80 g) was added, and the reaction mixture was stirred at 80° C. for 4 hr. Acetic acid/water/ethyl acetate were added to the reaction mixture, and the organic layer was separated, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) and washed with diethyl ether to give the title compound (7.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772277B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-9690bea49a354c56b701fe801f265ef5 |
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| Source note | uspto-grants-2014_07 |
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