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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
ReactantMethyl 3-methyl-5-nitrosalicylateHCID 12099450—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-methyl-5-nitro-2-trifluoromethylsulfonyloxybenzoateHCID 5802683696%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420635B2
Source datasetuspto-grants-2013_04
ORD IDord-8a26bedd2dce48e8b635e871ae5cd636
Source noteuspto-grants-2013_04