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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272490Generated: November 2, 2026

Potassium Carbonate → HCID 118038096, compound

https://huagongshe.com/reaction/2272490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzyloxy-2(1H)-pyridoneHCID 3607724—
Reactant1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 15734713—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 118038096HCID 11803809630.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120777B2
Source datasetuspto-grants-2015_09
ORD IDord-20758a1a845c4e84ba77e889087ad3b1
Source noteuspto-grants-2015_09