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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726273Generated: November 2, 2026

4-Fluorocatechol → HCID 68970624, compound

https://huagongshe.com/reaction/1726273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorocatecholHCID 160458—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactanttert-Butyl 4-(4-methoxybenzoyl)piperidine-1-carboxylateHCID 49760136—
SolventO-XyleneHCID 7237—
ProductHCID 68970624HCID 6897062433.4%

Reaction Steps

A solution of 4-(4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (see EXAMPLE 284) (638 mg, 2.00 mmol), 4-fluorocatechol (512 mg, 4.00 mmol) and p-TsOH.H2O (760 mg, 4.00 mmol) in xylene (20 mL) was heated at reflux using a Dean-Stark apparatus to remove water for 52 hours. Standard work-up and purification gave 4-[5-fluoro-2-(4-methoxy-phenyl)-benzo[1,3]dioxol-2-yl]-piperidine as a pale yellow oil (220 mg, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-94e480d75cd342819f588666288f3fb1
Source noteuspto-grants-2009_02