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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726272Generated: November 2, 2026

4-Fluorocatechol → HCID 68968782, compound

https://huagongshe.com/reaction/1726272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorocatecholHCID 160458—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 68971662HCID 68971662—
SolventO-XyleneHCID 7237—
ProductHCID 68968782HCID 6896878234%

Reaction Steps

A solution of 4-(4-methylsulfanyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (see EXAMPLE 28) (168 mg, 0.50 mmol), 4-fluorocatechol (128 mg, 2.0 mmol) and p-TsOH.H2O (190 mg, 1.0 mmol) in xylene (50 mL) was heated at reflux under a Dean-Stark trap for 41 hours. Standard work-up and purification gave 4-[5-fluoro-2-(4-methylsulfanyl-phenyl)-benzo[1,3]dioxol-2-yl]-piperidine as a white solid (58 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-22fe109083be4c8fbfe81a4f44da5880
Source noteuspto-grants-2009_02