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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733376Generated: November 1, 2026

4-Nitrobenzaldehyde → HCID 178502516, compound

https://huagongshe.com/reaction/1733376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantHCID 178502512HCID 178502512—
SolventBenzeneHCID 241—
ProductHCID 178502516HCID 178502516—

Reaction Steps

To a mixture of 3-amino-4-(3-carbomethoxy-S-methylisothioureido)benzophenone (3.43 g.; 0.01 mol) in benzene (100 ml.) there is added 4-nitrobenzaldehyde (1.5 g.; 0.01 mol). The mixture is refluxed and stirred for 3 hours. Water of the reaction is removed by a Dean-Stark distillation receiver. The mixture is poured into an excess of hexane and the suspension formed is vacuum filtered. The filter cake is dried to afford 3-imino-(4-nitrophenyl)methyl-4-(3-carbomethoxy-S-methylisothioureido)benzophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241079
Source datasetuspto-grants-1980_12
ORD IDord-8fcc5a6f20954fddb23140cb8fec8dfa
Source noteuspto-grants-1980_12