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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073602Generated: November 3, 2026

6,7,8-Trifluorocarbostyril → 6,7,8-Trifluoro-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1073602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6,7,8-TrifluorocarbostyrilHCID 19934872—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product6,7,8-Trifluoro-3,4-dihydrocarbostyrilHCID 5424573495.9%

Reaction Steps

24.35 g of 6,7,8-trifluorocarbostyril in suspension in a mixture of 450 cm3 of ethanol and 150 cm3 of dimethylformamide are hydrogenated, with stirring, at about 50° C., in the presence of 5 g of Raney nickel under a pressure of 1 atmosphere until the absorption of hydrogen has ceased. The W-2 grade Raney nickel used is washed beforehand with 50 cm3 of an aqueous 2% acetic acid solution, twice 50 cm3 of water and 3 times 50 cm3 of ethanol. 250 cm3 of dimethylformamide are added to the reaction mixture and the mixture is filtered at about 50 C. through diatomaceous silica. The filtrate is concentrated under reduced pressure (20 kPa) at about 70° C. The dry extract is taken up in 150 cm3 of water, drained and washed with twice 50 cm3 of water. 23.6 g of 6,7,8-trifluoro-3,4-dihydrocarbostyril are obtained in the form of a light beige solid melting at 217° C., which is used for the subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970213
Source datasetuspto-grants-1990_11
ORD IDord-00dab238f3a8425a962710c0fbb126ad
Source noteuspto-grants-1990_11