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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069260Generated: October 31, 2026

Methanol → Methyl 2-amino-5-nitro-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/2069260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant2-Amino-5-nitro-4-trifluoromethyl-benzoic acidHCID 18536731—
ProductMethyl 2-amino-5-nitro-4-(trifluoromethyl)benzoateHCID 1196577890%

Reaction Steps

A solution of 28 g (112 mmol) of 2-amino-5-nitro-4-trifluoromethyl-benzoic acid in 550 ml of methanol is cooled to 0° C. under nitrogen and concentrated H2SO4 is added dropwise in order to keep the temperature around 20° C. Upon completion of the addition, the mixture is heated to reflux for 24 hours. It is then allowed to cool to room temperature and the mixture is concentrated in vacuo to about 50 ml. This residue is poured onto ice and extracted with ethyl acetate. The organic phase is washed with a saturated aqueous solution of NaHCO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product is recrystallized in toluene to give 26.7 g (90%) of 2-amino-5-nitro-4-trifluoromethyl-benzoic acid methyl ester as yellow crystals, m.p. 174-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299085B2
Source datasetuspto-grants-2012_10
ORD IDord-78be601b9a8e42fa8d9b1c945c99f8c7
Source noteuspto-grants-2012_10