HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107274Generated: October 30, 2026
Dimethyl Sulfoxide → tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1107274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-t-Butyloxycarbonyl-3-hydroxy-2-phenylpiperidine | HCID 21584093 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate | HCID 11414684 | — |
Reaction Steps
To a cooled (-60° C.) solution of oxalyl chloride (0.68 ml, 7.8 mmol) in dichloronmethane (17 ml) was added dimethyl sulphoxide (0.69 ml, 9.8 mmol) for 10 minutes before addition of (±)1-tert-butoxycarbonyl-3-hydroxy-2-phenylpiperidine (1.8 g, 6.5 mmol; prepared by the method described in European Patent Specification number 0 528 495-A) in dichloromethane (7 ml). The solution was stirred at -60° C. for 20 minutes, warmed to -30° C. and triethylamine (2.5 ml) added. The solution was warmed to room temperature then was washed with ice cold 10% aqueous citric acid solution (40 ml, twice), water and dried (MgSO4). After evaporation the residue was purified by chromatography on silica gel (eluting with hexane containing an increasing proportion of ethyl acetate up to 20%) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06060469 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-7bfb5fe95396445f8219e89207c58322 |
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| Source note | uspto-grants-2000_05 |
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