HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862197Generated: October 29, 2026
Dimethyl Sulfoxide → 3,4-Dichlorophenyl-2-piperdin-4-yl-ethane-1,2-dione
https://huagongshe.com/reaction/862197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(3,4-Dichlorophenyl)-2-pyridin-4-yl-ethane-1,2-diol | HCID 22185450 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-Dichlorophenyl-2-piperdin-4-yl-ethane-1,2-dione | HCID 131720467 | 71.8% |
Reaction Steps
To a stirring solution of methyl sulfoxide (38.3 g, 35 mL, 490 mmol) in dichloromethane (750 mL) at -78° C. was added trifluoroacetic anhydride (77 g, 52 mL, 368 mmol) dropwise. After ten minutes, 1-(3,4-dichlorophenyl)-2-pyridin-4-yl-ethane-1,2-diol (31.7 g, 112 mmol) in dichloromethane (500 mL) was added dropwise. After another ten minutes, triethylamine (70 g, 96 mL, 690 mmol) was added dropwise and the reaction mixture immediately warmed to 0° C. and poured into saturated aqueous sodium hydrogen carbonate (300 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL) and the organic layers were combined, dried over anhydrous magnesium sulfate, filtered and concentrated at reduced pressure. The resulting solid was triturated with ethyl acetate to give the dione as a yellow solid (23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05717100 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-a256b20682034e6fa6cd678107f0f0bf |
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| Source note | uspto-grants-1998_02 |
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