HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012285Generated: October 30, 2026
Water → tert-Butyl 3-(tosyloxy)piperidine-1-carboxylate
https://huagongshe.com/reaction/1012285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Boc-3-hydroxypiperidine | HCID 545699 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | tert-Butyl 3-(tosyloxy)piperidine-1-carboxylate | HCID 20468243 | 28.3% |
Reaction Steps
To a solution of tert-butyl 3-hydroxypiperidine-1-carboxylate (2.00 g, 9.94 mmol) in chloroform (20 ml) were successively added p-toluenesulfonyl chloride (2.27 g, 11.9 mmol) and triethylamine (1.66 ml, 11.9 mmol) at 0° C., and the mixture was stirred at 70° C. for 9 hr. The reaction mixture was allowed to cool to room temperature, water was added to the reaction mixture and the mixture was extracted with chloroform. The organic layer was successively washed with water and saturated brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate:hexane=1:1) to give tert-butyl 3-(toluene-4-sulfonyloxy)piperidine-1-carboxylate (1.00 g, yield 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977331B1 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-df199b96dc60464aa19642e23f0ecc61 |
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| Source note | uspto-grants-2011_07 |
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