HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394341Generated: October 31, 2026
Chlorosulfonic acid → HCID 22676671, compound
https://huagongshe.com/reaction/1394341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 1-(4-Benzylpiperidin-1-yl)-2,2,2-trifluoroethanone | HCID 897795 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22676671 | HCID 22676671 | 41.3% |
Reaction Steps
A mixture of 1-(trifluoroacetyl)-4-benzylpiperidine (29.2 g, 108 mmol) and dichloromethane (10 ml) was added dropwise to chlorosulfonic acid (36 ml, 539 mmol) over period of 1 h at −10° C. The mixture was stirred at 0° C. for 1 h and then at room temperature for 1 h. The whole was poured into ice-water (500 ml). The mixture was extracted with dichloromethane (200 ml×2). The extracts were washed with 5% aqueous sodium bicarbonate (500 ml), saturated sodium chloride solution (500 ml) successively. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel 100 g, ethyl acetate/hexane=1/20 to 1/5) to obtain the title compound (16.5 g, 41%) as a colorless crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348324B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-c8e9776333d046daac2860ed335fd16a |
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| Source note | uspto-grants-2008_03 |
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