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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775539Generated: October 30, 2026

4-(Trifluoromethyl)benzaldehyde → HCID 66576888, compound

https://huagongshe.com/reaction/1775539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantHCID 66576808HCID 66576808—
ProductHCID 66576888HCID 66576888—

Reaction Steps

Compound 23 was synthesised following similar procedures outlined in Example 24 (Compound 19), using 4-trifluoromethylbenzaldehyde instead of 3-methylbenzaldehyde in Step 1. As a slightly modified procedure, in Step 2, the reaction mixture was filtered and following evaporation of the filtrate, purification of (3,5-dichloro-6-phenylpyridazin-4-yl)(4-(trifluoromethyl)phenyl)methanone was carried out by trituration of the solid residue in diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260381B2
Source datasetuspto-grants-2016_02
ORD IDord-eaa952510605446296637087f4647999
Source noteuspto-grants-2016_02