HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272490Generated: November 2, 2026
Potassium Carbonate → HCID 118038096, compound
https://huagongshe.com/reaction/2272490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxy-2(1H)-pyridone | HCID 3607724 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine | HCID 15734713 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 118038096 | HCID 118038096 | 30.5% |
Reaction Steps
Potassium tert-butoxide (5.05 g) was added at room temperature to a DME (70 mL) solution of 4-(benzyloxy)pyridin-2(1H)-one (7.55 g). The reaction mixture was stirred at room temperature for 10 minutes. Then, potassium carbonate (10.4 g) and tert-butyl 4-(((4-methylphenyl)sulfonyl)oxy)piperidine-1-carboxylate (20.0 g) were added thereto, and the mixture was stirred at 100 C for 1 day in a nitrogen atmosphere. Then, DME (30 mL) was added thereto, and the mixture was further stirred during the weekend at 100 C. Saturated saline was added to the reaction mixture, followed by extraction with ethyl acetate twice. The obtained organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (4.40 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120777B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-20758a1a845c4e84ba77e889087ad3b1 |
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| Source note | uspto-grants-2015_09 |
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