HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225788Generated: November 3, 2026
Sodium hydride → 3-Methyl-2-(trifluoromethylsulfonyloxy)benzoic acid methyl ester
https://huagongshe.com/reaction/2225788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzoic acid, 2-hydroxy-3-methyl-, methyl ester | HCID 31835 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methyl-2-(trifluoromethylsulfonyloxy)benzoic acid methyl ester | HCID 22498813 | — |
Reaction Steps
In an inert atmosphere, a stirred solution of 3-methylsalicylic acid methyl ester (9.96 g) in dichloromethane (150 mL) cooled in an ice bath, was treated portionwise with 55% sodium hydride dispersion in mineral oil (3.0 g). The mixture was stirred at 0° C. for 15 minutes, then trifluoromethyl sulfonic acid (18.65 mL) was added dropwise over 20 minutes. The cooling bath was removed and the reaction was allowed to proceed for an additional hour. Water (75 mL) was added and the phases were separated. The organic layer was washed in turn with 10% potassium carbonate (75 mL) and with brine. The dried (Na2SO4) organic layer was evaporated and the resulting amber oil was purified by HPLC (diethyl ether-hexane; 1:4) to yield 14.3 g of 3-methyl-2-(trifluoromethylsulfonyloxy)benzoic acid methyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344843 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-35cb26d6b80a4356a6092a1ac2696fb9 |
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| Source note | uspto-grants-1994_09 |
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