HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → HCID 68970470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | tert-Butyl 4-(4-(trifluoromethoxy)benzoyl)piperidine-1-carboxylate | HCID 68968884 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 68970470 | HCID 68970470 | 71.2% |
Reaction Steps
A solution of 4-(4-trifluoromethoxy-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (see EXAMPLE 247) (373 mg, 1.0 mmol), catechol (440 mg, 4.0 mmol) and p-TsOH.H2O (380 mg, 2.0 mmol) in xylene (10 mL) was heated at reflux under a Dean-Stark trap for 44 hours. Standard work-up and purification gave 4-[2-(4-trifluoromethoxy-phenyl)-benzo[1,3]dioxol-2-yl]-piperidine as a white solid (260 mg, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491735B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-a799f2680a344b7ca6dda5d94f51be1b |
| Source note | uspto-grants-2009_02 |