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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710041Generated: October 31, 2026

Benzoyl chloride → HCID 19860973, compound

https://huagongshe.com/reaction/1710041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 23035205HCID 23035205—
SolventPyridineHCID 1049—
ProductHCID 19860973HCID 1986097320.2%

Reaction Steps

To a stirred mixture of 3 parts of 2,6-dichloro-α-(4-chlorophenyl)-4-(3,4,5,6-tetrahydro-4-methyl-3,5-dioxo-1,2,4-triazin-2(1H)-yl)benzeneacetonitrile and 20 parts of pyridine were added dropwise 1.7 parts of benzoyl chloride during a period of 5 minutes at room temperature and under nitrogen atmosphere. Upon complete addition, stirring was continued overnight at room temperature. The reaction mixture was evaporated 1n vacuo and the residue was stirred in water. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified twice by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was crystallized from 8 parts of acetonitrile. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 0.8 parts (20.2%) of 1-benzoyl-2-[3,5-dichloro-4-[(4-chlorophenyl)cyanomethy]phenyl]-1,6-dihydro-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione; mp. 148.4° C. (compound 79).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952570
Source datasetuspto-grants-1990_08
ORD IDord-fe7c720db9df498bb0f47ab6f81cb529
Source noteuspto-grants-1990_08