HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966273Generated: October 26, 2026
Water → Methyl 3-methyl-5-nitro-2-trifluoromethylsulfonyloxybenzoate
https://huagongshe.com/reaction/1966273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonyl chloride | HCID 79000 | — |
| Reactant | Methyl 3-methyl-5-nitrosalicylate | HCID 12099450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-methyl-5-nitro-2-trifluoromethylsulfonyloxybenzoate | HCID 58026836 | 96% |
Reaction Steps
Methyl 2-hydroxy-3-methyl-5-nitrobenzoate (Reference Compound No. 1-4-(2), 6.0 g, 28.4 mmol) was dissolved in tetrahydrofuran (200 mL), then triethylamine (16.7 mL, 120 mmol) and trifluorometanesulfonyl chloride (6.23 mL, 58.5 mmol) were added thereto, and then the reaction mixture was stirred at room temperature overnight. Water (500 mL) was added to the reaction mixture, then the whole was extracted with ethyl acetate (500 mL). The organic layer was washed with 0.2N aqueous NaOH solution (200 mL, twice) and saturated brine (200 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (9.32 g) as a pale yellow oil. (Yield 96%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420635B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-8a26bedd2dce48e8b635e871ae5cd636 |
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| Source note | uspto-grants-2013_04 |
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