HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003252Generated: October 30, 2026
Dimethyl Sulfoxide → (2S)-1-tert-butoxycarbonyl-2-phenylpiperidin-3-one
https://huagongshe.com/reaction/1003252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2S,3S)-1-t-Butyloxycarbonyl-3-hydroxy-2-phenylpiperidine | HCID 10901890 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S)-1-tert-butoxycarbonyl-2-phenylpiperidin-3-one | HCID 10956740 | — |
Reaction Steps
To a cooled (-60° C.) solution of oxalyl chloride (0.68 ml, 7.8 mmol) in dichloromethane (17 ml) was added dimethyl sulfoxide (0.69 ml, 9.8 mmol) over 10 minutes before addition of (2S,3S)1-tert-butoxycarbonyl-3-hydroxy-2-phenylpiperidine (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 0° C. then was washed with ice cold 10% aqueous citric acid solution (40 ml, twice) water and dried (MgSO4). The solution was evaporated to dryness to give the title compound and this was used immediately without further purification. 1H NMR (250 MHz, CDCl3) δ 7.5-7.3 (5H,m), 5.8 (1H, bs), 4.2 (1H, bs), 3.4 (1H, m), 2.6 (2H, m), 2.0 (2H, m), 1.54 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046195 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-e64f50b7296d474ab7814b34de0041fc |
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| Source note | uspto-grants-2000_04 |
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