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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274512Generated: October 30, 2026

Ethanol → Ethyl(3,4-dihydroxy-5-nitrobenzoyl)acetate

https://huagongshe.com/reaction/274512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBoron tribromideHCID 25134—
ReactantDiethyl 3,4-dimethoxy-5-nitrobenzoylmalonateHCID 19000155—
SolventDichloromethaneHCID 6344—
ProductEthyl(3,4-dihydroxy-5-nitrobenzoyl)acetateHCID 21459116—

Reaction Steps

20.1 g of diethyl (3,4-dimethoxy-5-nitrobenzoyl)-malonate are dissolved in 200 ml of methylene chloride, whereupon the solution is cooled to -20° and at this temperature there is added dropwise while stirring within 15 minutes a solution of 68.1 g of boron tribromide in 120 ml of methylene chloride. The mixture is subsequently stirred at room temperature overnight. After cooling to -20° , the mixture is treated with 300 ml of ethanol and stirred at room temperature for 30 minutes. The solvent is distilled in a water-jet vacuum at 40° . The residue is treated with 300 ml of ice-water and methylene chloride. The organic phase is washed with water, dried over sodium sulfate and evaporated. The crude product obtained is chromatographed on a 10-fold amount of silica gel with toluene. After crystallization from methylene chloride/hexane there is obtained ethyl (3,4-dihydroxy-5-nitrobenzoyl)acetate in the form of yellow crystals of m.p. 136°-137°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-f4c4085356fe4424b02fec0fd474e987
Source noteuspto-grants-1995_02