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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112382Generated: November 2, 2026

4-Hydroxy-3,5-dinitrobenzaldehyde → HCID 22763893, compound

https://huagongshe.com/reaction/1112382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-3,5-dinitrobenzaldehydeHCID 104091—
ReactantHCID 22763917HCID 22763917—
ReactantHCID 178526649HCID 178526649—
ProductHCID 22763893HCID 22763893—

Reaction Steps

Compounds in which the substituent in the 6(5) position of the benzene ring of the benzimidazole is difluoromethyl are prepared from 2,6-dinitro-4-difluoromethylbenzene according to the above procedure. This latter compound is prepared by the reaction of SF4 and 3,5-dinitro-4-hydroxybenzaldehyde to yield 2,6-dinitro-4-difluoromethylphenol which is converted to the corresponding chloride by conventional means. 2-Trifluoromethyl-4-nitro-6-difluoromethylbenzimidazole was prepared from the above diamine by the process of the above example and melted at about 132°-134° C. after recrystallization from benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04122184
Source datasetuspto-grants-1978_10
ORD IDord-71a54c7f266a4bdca8fd9ba0c68a4e60
Source noteuspto-grants-1978_10