HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620467Generated: November 1, 2026
tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 178482474, compound
https://huagongshe.com/reaction/1620467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178482466 | HCID 178482466 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178482474 | HCID 178482474 | 51.7% |
Reaction Steps
tert-Butyl 4-formylpiperidine-1-carboxylate (1.61 g) and 4-(methylamino)-1,3-thiazol-2(5H)-one (1.18 g) were suspended in ethanol (10 mL), potassium tert-butoxide (1.02 g) was added, and the mixture was stirred at 80° C. for 8 hr. The reaction mixture was concentrated, saturated aqueous ammonium chloride solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with 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 (NH, ethyl acetate/hexane) to give the title compound (1.27 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-a2ab593111f2466c8984bed50b0ee5f8 |
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| Source note | uspto-grants-2014_07 |
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