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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406541Generated: October 30, 2026

Ethanol → Ethyl 4-amino-2-ethoxy-5-nitro-benzoate

https://huagongshe.com/reaction/1406541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDichloromethaneHCID 6344—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantEthyl 4-amino-2-fluoro-5-nitrobenzoateHCID 59529828—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-amino-2-ethoxy-5-nitro-benzoateHCID 67230429—

Reaction Conditions

Temperature60 °C

Reaction Steps

KHMDS (1.92 g, 9.64 mmol) was added to a mixture of ethyl 4-amino-2-fluoro-5-nitro-benzoate (2.00 g, 8.77 mmol) and ethanol (0.56 mL, 9.64 mmol) in 70 mL THF at 0° C. The mixture was stirred at 60° C. for 16 h. Then KHMDS (1.92 g, 9.64 mmol) and ethanol (1.2 mL, 20.7 mmol) were added at ambient temperature and the mixture was stirred at 60° C. for 2 h. 100 mL dichloromethane were added and the mixture extracted with sat. NH4Cl (aq). The organic layer was evaporated, the residue mixed with ethyl acetate, washed with sat. NaCl (aq), dried over Na2SO4, filtered and evaporated. The residue was purified twice by chromatography (silica gel; eluens: petrol ether/ethyl acetate=1:1 and 2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916599B2
Source datasetuspto-grants-2014_12
ORD IDord-fb248388f9c54bc8ba9663aaa49a0ced
Source noteuspto-grants-2014_12