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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165854Generated: November 4, 2026

2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-alpha-(4-fluorophenyl)-alpha-methylbenzeneacetonitrile → HCID 23035207, compound

https://huagongshe.com/reaction/1165854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-alpha-(4-fluorophenyl)-alpha-methylbenzeneacetonitrileHCID 13770340—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 23035207HCID 2303520753.6%

Reaction Steps

To a stirred and refluxed mixture of 1.5 parts of 2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl) -α-(4-fluorophenyl)-α-methylbenzeneacetonitrile and 75 parts of acetic acid were added portionwise 3 parts of zinc during a period of 30 minutes. Upon complete addition, stirring was continued for 3 hours at reflux. The reaction mixture was filtered while hot and the filtrate was concentrated in vacuo to 10 parts of its volume. Water was added to the concentrate. The precipitated product was filtered off and purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and eluent was evaporated in vacuo. The residue was crystallized from acetonitrile. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 0.8 parts (53.6%) of 2-chloro-α-(4-fluorophenyl)-α-methyl-4-(3,4,5,6-tetrahydro-3,5-dioxo-1,2,4-triazin-2(1H)-yl)benzeneacetonitrile; mp. 122.5° C. (compound 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912106
Source datasetuspto-grants-1990_03
ORD IDord-b64fe672ff6e4bde883211ca90559c0d
Source noteuspto-grants-1990_03