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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198826Generated: November 3, 2026

3-Fluorobenzaldehyde → HCID 13064591, compound

https://huagongshe.com/reaction/2198826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzaldehydeHCID 68009—
ReactantHCID 13059651HCID 13059651—
SolventEthanolHCID 702—
ProductHCID 13064591HCID 13064591—

Reaction Steps

A 7.0 g. amount of N'-(4-amino-2,6-dichlorophenyl)-N,N-dimethylformamidine (Example 9) is dissolved in 25 ml. of absolute ethanol then 3.7 g. of m-fluorobenzaldehyde is added and the mixture is refluxed for one hour. The solution is evaporated to an amber syrup which crystallizes. The material is dissolved in 50 ml. of refluxing ether and hexane is added until turbidity results. The crystalline product is collected and washed with hexane. The product is recrystallized from ether/hexane to give 1.4 g. of the product of the Example as hard yellow crystals, m.p. 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360466
Source datasetuspto-grants-1982_11
ORD IDord-82b230fd884d4b549345f88975a721f8
Source noteuspto-grants-1982_11