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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958062Generated: October 25, 2026

Methanol → Methyl 2-methyl-3-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/1958062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methyl-3-(trifluoromethyl)benzoic acidHCID 2775584—
ProductMethyl 2-methyl-3-(trifluoromethyl)benzoateHCID 1783761988%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a 500 mL round bottom equipped with an Airflux Condenser and stir bar was added 2-methyl-3-(trifluoromethyl)benzoic acid (30 g, 147 mmol). The solid was taken up in Methanol (101 ml) and to that solution was slowly added sulfuric acid (8.22 ml, 154 mmol). The reaction was then fitted with the condenser and heated to 75° C. overnight. The reaction was cooled back to room temperature, and neutralized by slow addition of 1N NaOH (˜155 mL). The solution was then extracted with 3×300 mL Et2O, the organic layer dried over magnesium sulfate, and concentrated to an oil, which solidified under vacuum to give off white solid methyl 2-methyl-3-(trifluoromethyl)benzoate (28.25 g, 129 mmol, 88% yield) 1H NMR (400 MHz, DMSO-d6) δ ppm 2.54 (d, J=1.77 Hz, 3H) 3.89 (s, 3H) 7.53 (t, J=7.83 Hz, 1H) 7.89 (d, J=7.83 Hz, 1H) 7.97 (d, J=7.83 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410095B2
Source datasetuspto-grants-2013_04
ORD IDord-6214d59bf0ce4ebd85438c384756db5f
Source noteuspto-grants-2013_04