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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Methyl-3-(trifluoromethyl)benzoic acid | HCID 2775584 | — |
| Product | Methyl 2-methyl-3-(trifluoromethyl)benzoate | HCID 17837619 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410095B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-6214d59bf0ce4ebd85438c384756db5f |
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| Source note | uspto-grants-2013_04 |
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