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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074230Generated: November 1, 2026

Acetonitrile → HCID 57507753, compound

https://huagongshe.com/reaction/2074230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorobenzyl bromideHCID 68007—
Reactant1-tert-Butoxycarbonyl-4-[(4-hydroxyphenyl)sulfanyl]piperidineHCID 18538757—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57507753HCID 57507753—

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(Bromomethyl)-3-fluorobenzene (0.436 ml) and potassium carbonate (670 mg) were added to an acetonitrile (15 ml) solution containing tert-butyl 4-[(4-hydroxyphenyl)sulfanyl]piperidine-1-carboxylate (1.00 g), followed by heating at 80° C. for 2 hours. The reaction solution was cooled, saturated brine was added thereto, followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=8:1 (v/v)) to obtain tert-butyl 4-({4-[(3-fluorobenzyl)oxy]phenyl}sulfanyl)piperidine-1-carboxylate (1.50 g) as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919494B2
Source datasetuspto-grants-2011_04
ORD IDord-dc5b50e8d0b749e597a73160dd179cf4
Source noteuspto-grants-2011_04