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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913290Generated: November 1, 2026

Hydrochloric Acid → 2-Hydroxy-3-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1913290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant1-Methoxymethoxy-2-(trifluoromethyl)benzeneHCID 10943639—
ReactantButyllithiumHCID 178418339—
Product2-Hydroxy-3-(trifluoromethyl)benzoic acidHCID 1088903999%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of Example 42A (14.1 g, 68.4 mmol) in THF (68 mL) was cooled to −20° C. and n-butyllithium (30.1 mL of a 2.5 M solution in hexanes, 75.0 mmol) was added slowly, keeping the temperature at 0° C. After 70 min at −5 to 5° C., the reaction mixture was cooled to −20° C. and CO2 gas was bubbled through the brown slurry, keeping the temperature ≦−10° C. The reaction went from a brown slurry to a dark purple solution to a yellow solution. After 10 min, the reaction mixture was cooled further to −20° C. and treated with 2N HCl (68 mL, 140 mmol). To facilitate the reaction mixture, additional concentrated HCl (17 mL, total 5 equiv of 4M HCl) was added. After 30 min, MTBE (70 mL) was added, and the organic portion was extracted with 2N NaOH (70 mL) and water (70 mL). The aqueous layer was acidified with 2N HCl (98 mL) and extracted with dichloromethane (2×140 mL). The organic portion was dried (Na2SO4), filtered, and concentrated to give the title compound (14.8 g, 71.8 mmol, 99%) as a yellow solid which was used without further purification. MS (DCI/NH3) m/z 207 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609692B2
Source datasetuspto-grants-2013_12
ORD IDord-a94060dd2e874f69a0f43c68f33bf18b
Source noteuspto-grants-2013_12