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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967620Generated: October 31, 2026

Methyl 5-nitro-2-(trifluoromethoxy)benzoate → Methyl 5-amino-2-(trifluoromethoxy)benzoate

https://huagongshe.com/reaction/967620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-nitro-2-(trifluoromethoxy)benzoateHCID 46311174—
SolventEthanolHCID 702—
ProductMethyl 5-amino-2-(trifluoromethoxy)benzoateHCID 2206115575.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

5-Nitro-2-trifluoromethoxybenzoic acid methyl ester (5.69 g, 21.5 mmol) was dissolved in ethanol 99.9% (80 mL) and added stannous(II)chloride dihydrate (24.2 g, 107 mmol). The suspension was stirred at 75° C. for 2 hours and then concentrated in vacuo. The residue was added ethyl acetate (100 mL) and water (50 mL) and pH was adjusted to pH 8 with 4 N sodium hydroxide (50 mL). The liquid was decanted from the fine precipitation, which occurred, and the precipitation was washed with ethyl acetate and decanted twice. The combined organic phases were washed with water saturated sodium chloride (1:1) solution (2×100 mL), dried (magnesium sulphate) and concentrated in vacuo. The residue was purified by column chromatography (120 g silica) using ethyl acetate:heptane (1:1) as eluent to give 3.8 g of 5-amino-2-trifluoromethoxybenzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953812B2
Source datasetuspto-grants-2005_10
ORD IDord-860e2bb48ca941e094d4b0615b2f7ee5
Source noteuspto-grants-2005_10