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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595634Generated: October 31, 2026

Nitric Acid → Ethyl 5-bromo-6-nitrobenzofuran-3-carboxylate

https://huagongshe.com/reaction/595634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantEthyl 5-bromo-1-benzofuran-3-carboxylateHCID 21694192—
SolventChloroformHCID 6212—
ProductEthyl 5-bromo-6-nitrobenzofuran-3-carboxylateHCID 9033239285%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 5-bromobenzofuran-3-carboxylate (95 g, 353 mmol) in CHCl3 (1000 mL), fuming HNO3 (192 mL, 95%) was added dropwise at −20° C. over 90 min and stirred at 0° C. for 1 hour. The reaction mixture was added to ice water and extracted with CH2Cl2. The organic layer was washed with NaHCO3 and brine. The solvent was removed by distillation to provide the crude product of ethyl 5-bromo-6-nitrobenzofuran-3-carboxylate (95 g, yield: 85%). It was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243002B2
Source datasetuspto-grants-2016_01
ORD IDord-dc6e4dde080c4b7c89c5f557cae5ea7f
Source noteuspto-grants-2016_01