HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752023Generated: October 28, 2026
Potassium Carbonate → HCID 67367623, compound
https://huagongshe.com/reaction/1752023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Trifluorophenol | HCID 519974 | — |
| Reactant | 4-(2-Methanesulfonyloxymethylphenyl)piperidine-1-carboxylic Acid t-Butyl Ester | HCID 46213046 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67367623 | HCID 67367623 | 86.1% |
Reaction Steps
4-(2-Methanesulfonyloxymethylphenyl)piperidine-1-carboxylic acid t-butyl ester (27.0 g, 60.6 mmol, 1.0 eq.) was dissolved in MeCN (540 mL) and added to K2CO3 (25 g, 180 mmol, 3.0 eq.) and 2,4,6-trifluorophenol (13.5 g, 90.9 mmol, 1.5 eq.). The mixture was vigorously stirred at 50° C. for 6 hours, removed from the heat, and stirred overnight. The mixture was cooled at room temperature, and diluted with EtOAc (700 mL) and water (700 mL). The phases were separated, and the organic layer was washed twice with 1.0 M NaOH in water (2×400 mL) and saturated aqueous NaCl (1×400 mL), then dried over Na2SO4 and the solvent removed to yield crude 4-[2-(2,4,6-trifluorophenoxymethyl)-phenyl]piperidine-1-carboxylic acid t-butyl ester (25.0 g). The crude product was combined with smaller scale runs for a total of 30 g, and purified by chromatography (0-10% EtOAc in hexanes) to yield 4-[2-(2,4,6-trifluorophenoxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester (22.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09162982B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-4259a3fbd2294919bbe6687c53a8187f |
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| Source note | uspto-grants-2015_10 |
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