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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633934Generated: October 31, 2026

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

https://huagongshe.com/reaction/1633934

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 4N 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 (MgSO4) 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 numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-50c65e5478a64131a173f981e74bd8e8
Source noteuspto-grants-2003_01