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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412465Generated: October 30, 2026

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

https://huagongshe.com/reaction/412465

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 stannous (II) chloride dihydrate (24.2 g, 107 mmol) was added. The suspension was stirred on an oil-bath at 75° C for 2 hours and concentrated in vacuo. Ethyl acetate (100 mL) and water (50 mL) was added and pH was adjusted to pH 8 with 4 N sodium hydroxide (50 mL). The liquid was decanted from the precipitation. The precipitate was washed twice with ethyl acetate. The aqueous phase was extracted twice with ethyl acetate (60 mL). The combined organic phases were washed with a saturated sodium chloride solution (2×100 mL), dried (magnesium sulphate) and concentrated in vacuo. Purification by column chromatography (120 g silica) using ethyl acetate and heptane (1:1) as eluent afforded 3.8 g of 5-amino-2-trifluoromethoxybenzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562807B2
Source datasetuspto-grants-2003_05
ORD IDord-f1e8da5c88fa4c26b3fb4e430069115f
Source noteuspto-grants-2003_05