HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862199Generated: October 26, 2026
Dimethyl Sulfoxide → 1-(3-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-dione
https://huagongshe.com/reaction/862199
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-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-diol | HCID 18704770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-dione | HCID 18704760 | 62.2% |
Reaction Steps
To a stirring solution of methyl sulfoxide (11.8 g, 10.7 mL, 150 mmol) in dichloromethane (150 mL) at -78° C. was added trifluoroacetic anhydride (23.7 g, 16 mL, 113 mmol) dropwise. After ten minutes, 1-(3-methoxyphenyl)-2-pyridin-4-ylethane-1,2-diol (8.5 g, 34 mmol) in dichloromethane (60 mL) was added dropwise. After another ten minutes, triethylamine (21.3 g, 29.4 mL, 211 mmol) was added dropwise and the reaction mixture was immediately warmed to 0° C. and poured into saturated aqueous sodium hydrogen carbonate solution (300 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL) and the organic layers were combined, dried over anhydrous magnesium sulfate and concentrated at reduced pressure. The resulting oil was chromatographed on silica gel eluting with 1:3 ethyl acetate:hexane to give the dione as a yellow solid (5.1 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-1ff64f2b09984fcdad44407e63bd6648 |
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| Source note | uspto-grants-1998_02 |
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