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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814659Generated: November 2, 2026

Nitric Acid → Methyl 5-nitro-2-(trifluoromethoxy)benzoate

https://huagongshe.com/reaction/1814659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantMethyl 2-(trifluoromethoxy)benzoateHCID 2775550—
ProductMethyl 5-nitro-2-(trifluoromethoxy)benzoateHCID 46311174—

Reaction Conditions

Temperature60 °C

Reaction Steps

Fuming nitric acid (5 mL) was cooled on an ice bath. Methyl 2-(trifluoromethoxy)benzoate (5 g, 22.7 mmol) was slowly added within 30 minutes keeping the temperature below 15° C. The reaction was then stirred at 60° C. for 1 hour and 2 hours at room temperature. The mixture was poured on ice water whereupon an oil separated. The aqueous supernatant was decanted and additional water (50 mL) was added to the oil. After neutralisation with sodium hydrogen carbonate, the mixture was extracted with ethyl acetate (25 mL). The aqueous phase was extracted with ethyl acetate (15 mL) once more. The combined organic phases were washed with saturated sodium chloride (2×15 mL), dried (MgSO4), and concentrated in vacuo to give 5.69 g of 5-nitro-2-trifluoromethoxybenzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875760B2
Source datasetuspto-grants-2005_04
ORD IDord-8edbb7f83dc34b0288491f22097241d9
Source noteuspto-grants-2005_04