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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763623Generated: November 1, 2026

Trifluoroacetic acid → HCID 20310365, compound

https://huagongshe.com/reaction/1763623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 20310370HCID 20310370—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 20310365HCID 20310365—

Reaction Steps

A mixture 10 g. of 6-[4-nitro-3-(trifluoromethyl)phenyl]-3(2H)-pyridazinone in 50 ml. of trifluoroacetic acid is reduced with hydrogen and palladium on carbon to give 6-[4-amino-3-(trifluoromethyl)phenyl]-3(2H)-pyridazinone. The preceding compound is converted to 6-[4-fluoro-3-(trifluoromethyl)phenyl]-3(2H)-pyridazinone by the procedure described in J. Org. Chem., 26, 468 (1961). The preceding compound is reacted with phosphorus oxychloride as described in Example 47 to give 3-chloro-6-[4-fluoro-3-(trifluoromethyl)phenyl]pyridazine., which is reacted with formylhydrazine as described in Example 48 to give the product of the example.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112095
Source datasetuspto-grants-1978_09
ORD IDord-5a5420ccdab845d0998e00e9d056e977
Source noteuspto-grants-1978_09