HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585464Generated: November 1, 2026
Pyridine → Methyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoate
https://huagongshe.com/reaction/1585464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Methyl 3-hydroxy-4-methanesulfonyl-2-methylbenzoate | HCID 18694846 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoate | HCID 18694857 | 99.6% |
Reaction Steps
8.8 g (0.036 mol) of methyl 3-hydroxy-4-methanesulfonyl-2-methyl-benzoate was dissolved in 100 ml of methylene chloride, and 8.3 g (0.11 mol) of pyridine was added. After the solution was cooled to 0° C., 12.2 g (0.043 mol) of anhydrous trifluoromethanesulfonic acid was added. After stirring at room temperature for 1 hour, the reaction mixture was washed with 1N hydrochloric acid and subsequently with saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 13.5 g of methyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoate. Yield=99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05939360 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-7719549e4b174447b74d31accaeae9a0 |
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| Source note | uspto-grants-1999_08 |
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