HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070982Generated: October 31, 2026
Dimethyl Sulfoxide → 1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-one
https://huagongshe.com/reaction/1070982
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-ol | HCID 22398501 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-one | HCID 22398487 | 86.5% |
Reaction Steps
A solution of 516 μL (1.03 mmol, 1.2 eq) of oxalyl chloride (2.0 M solution in dichloromethane) was diluted with 2 mL of dichloromethane. To this solution was added a solution of 146 μL (2.06 mmol, 2.4 eq.) of DMSO in 0.2 mL of dichloromethane at −60° C. and the mixture was stirred for 10 minutes at this temperature. Then to this mixture was added a solution of 200 mg (0.86 mmol) of 1,1,1-trifluoro-4-methyl-4-pyridin-2-ylpentan-2-ol in 2 mL of dichloromethane at −60° C. The resulting mixture was stirred at −60° C. for 15 minutes and then 600 μL (4.3 mmol, 5.0 eq.) of triethylamine was added. The cooling bath was removed and the reaction mixture was allowed to warm to room temperature and quenched with water. The organic layer was separated. The aqueous layer was extracted three times with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography, providing 172 mg (86%) 1,1,1-trifluoro-4-methyl-4-pyridin-2-ylpentan-2-one as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903215B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-3ea14397c2c642968a4f118bafc7acf8 |
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| Source note | uspto-grants-2005_06 |
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