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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726249Generated: October 31, 2026

Catechol → HCID 68968790, compound

https://huagongshe.com/reaction/1726249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 68971662HCID 68971662—
SolventO-XyleneHCID 7237—
ProductHCID 68968790HCID 6896879087.3%

Reaction Steps

A solution of 4-(4-methylsulfanyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (see EXAMPLE 28) (335 mg, 1.0 mmol), catechol (440 mg, 4.00 mmol) and p-TsOH.H2O (380 mg, 2.00 mmol) in xylene (10 mL) was heated at reflux under a Dean-Stark trap for 45 hours. Standard work-up and purification gave 4-[2-(4-methylsulfanyl-phenyl)-benzo[1,3]dioxol-2-yl]-piperidine as a white solid (286 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-e395ff38307241ab9a9dde00692f18bb
Source noteuspto-grants-2009_02