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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330481Generated: October 29, 2026

Benzaldehyde → 3230-49-7

https://huagongshe.com/reaction/330481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant2-Amino-4-NitrophenolHCID 3613389—
SolventEthanolHCID 702—
Product3230-49-7HCID 270036—

Reaction Steps

A solution of 6.16 g of 2-amino-4-nitrophenol and 4.77 g of benzaldehyde in ethanol is refluxed. The reaction solution is condensed and cooled. The crystalline precipitates are collected by filtration to give 2-benzylideneamino-4-nitrophenol. 15.5 g of lead tetraacetate are added to a benzene suspension of the product obtained above, and the mixture is stirred. After the reaction, insoluble materials are filtered off. The filtrate is washed, and condensed. The residue is purified by silica gel column chromotography and recrystallized from ethanol, whereby 5.08 g of 5-nitro-2-phenylbenzoxazole are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897393
Source datasetuspto-grants-1990_01
ORD IDord-f181a0a32035429fa2b8d8f4179ab4b3
Source noteuspto-grants-1990_01