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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274441Generated: October 26, 2026

3,4-Dimethoxy-5-nitrobenzhydrol → 3,4-Dimethoxy-5-nitrobenzophenone

https://huagongshe.com/reaction/274441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxy-5-nitrobenzhydrolHCID 21458992—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product3,4-Dimethoxy-5-nitrobenzophenoneHCID 21459055—

Reaction Steps

2.5 g of 3,4-dimethoxy-5-nitrobenzhydrol dissolved in 50 ml of methylene chloride are treated with 2.2 g of pyridinium chlorochromate, whereupon the mixture is stirred at room temperature for 2 hours. The insoluble constituents are subsequently filtered. The filtrate is evaporated and the residue is chromatographed on 60 g of silica gel with methylene chloride. After crystallization from methylene chloride/hexane there is obtained 3,4-dimethoxy-5-nitrobenzophenone of m.p. 78°-80°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-df04f892a15b4ff9a9ea3a10b0f09001
Source noteuspto-grants-1995_02