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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781812Generated: November 1, 2026

Ethanol → Ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate

https://huagongshe.com/reaction/1781812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSelenium DioxideHCID 24007—
Reactant2-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenoneHCID 14450983—
ProductEthyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylateHCID 14450984—

Reaction Steps

ba) A suspension of 580.1 mg of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone in 10 ml of ethanol is treated with 443.8 mg of selenium dioxide and heated under reflux for 71 hours. Thereafter, the selenium is removed by filtration and the filtrate is evaporated. The residue is dissolved in methylene chloride, washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. There is obtained ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate of m.p. 165°-167° (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-657381fee6594bcc800e24778971091f
Source noteuspto-grants-1997_05