HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412882Generated: October 29, 2026
Trifluoromethanesulfonic acid → HCID 21906096, compound
https://huagongshe.com/reaction/412882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21906096 | HCID 21906096 | — |
Reaction Steps
To a solution of 1-tert-butoxycarbonyl-4-hydroxypiperidine (1.01 g, 5.0 mmol)and diisopropylethylamine (2.6 mL, 15 mmol)in dry dichloromethane (30 mL) was added anhydrous trifluoromethanesulfonic acid (1.0 mL, 6.0 mmol) at −78° C. The mixture was stirred for 1 minute under ice cooling, and cooled to −78° C. To the reaction mixture was added 2-mercaptopyridine (1.67 g, 15 mmol), and the mixture was stirred at room temperature for 20 hours. To the reaction mixture was added a saturated aqueous solution of sodium hydrogencarbonate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous solution of sodium hydrogen carbonate and saturated aqueous solution of sodium chloride, successively, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (50 g, ethyl acetate-hexane 1:5) to give the titled compound as pale yellow oily substance (937 mg, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562978B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-519209f92a3543ffa1b6776c43b945ec |
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| Source note | uspto-grants-2003_05 |
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