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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520811Generated: October 31, 2026

4-Hydroxybenzaldehyde → tert-Butyl 4-(4-formylphenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/520811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 15734713—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(4-formylphenoxy)piperidine-1-carboxylateHCID 22632605100.4%

Reaction Steps

A solution of 4-Hydroxybenzaldehyde (20.1 grams, 0.164 moles), potassium carbonate (67.9 grams, 0.492 moles) and t-butyl 4-(toluene-4-sulfonyloxy)piperidine-1-carboxylate (70 grams, 0.197 moles) in acetonitrile (1000 mL) was stirred for 18 hours at 80° C. The progress of the reaction was monitored by thin layer chromatography. After completion of reaction, the mass was cooled to room temperature and quenched on to chilled water (1000 mL). The compound was extracted with dichloromethane (3×500 mL). The resulting dichloromethane layer was washed with 10% lye solution (100 mL), water (100 mL) and brine solution (100 mL). The organic phase was dried over sodium sulfate and concentrated under reduced pressure to afford the title compound (50.3 grams).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328092B2
Source datasetuspto-grants-2016_05
ORD IDord-c0f5579d3d1e4cca9970e82b5ddb39bb
Source noteuspto-grants-2016_05