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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272276Generated: October 30, 2026

Nitric Acid → HCID 67355479, compound

https://huagongshe.com/reaction/2272276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantHCID 67354738HCID 67354738—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 67355479HCID 6735547932%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-(4-chlorophenyl)-5-isopropoxybenzofuran-3-carboxylate 4 (30 g, 0.084 mol) was dissolved in chloroform (75 mL) and the resulting solution was cooled in an ice bath. Nitric acid (55 mL) was also dissolved in chloroform (75 mL) and cooled in an ice bath. The acid solution was added dropwise to the solution of ethyl 2-(4-chlorophenyl)-5-isopropoxybenzofuran-3-carboxylate over 1 hour, and the reaction mixture was then stirred at 0° C. for 1.5 hrs. The reaction mixture was then diluted with water (60 mL) and the layers were separated. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give a brown oil which was purified by column chromatography (5/1 PE/EA) to afford ethyl 2-(4-chlorophenyl)-5-isopropoxy-6-nitrobenzofuran-3-carboxylate as a brown solid (11 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119868B2
Source datasetuspto-grants-2015_09
ORD IDord-7d566a8461784e73bfd65c95d8729a77
Source noteuspto-grants-2015_09