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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984040Generated: October 29, 2026

Water → HCID 22557413, compound

https://huagongshe.com/reaction/984040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,6-dichloro-alpha-(4-chlorophenyl)-4(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)benzeneacetylchlorideHCID 22557320—
ReactantHCID 178507064HCID 178507064—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22557413HCID 2255741317.3%

Reaction Conditions

Temperature-75 °C

Reaction Steps

A mixture of 2,6-dichloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4,-triazin-2(3H)-yl)-benzeneacetyl chloride (0.05 mol) in THF (200 ml) was stirred at −75° C. A solution of chloroethyl magnesium (0.1 mol; 2 M/THF) in THF (50 ml) was added dropwise at −75° C. The reaction mixture was stirred for 90 minutes, then the temperature was raised to −20° C. A saturated aqueous NH4Cl solution was added dropwise. Water was added and the product was extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was filtered over silica gel (eluent: CH2Cl2/CH3OH 98/2). Two fractions were collected and the solvent was evaporated, yielding 3.8 g (±)-2-[3,5-dichloro-4-[1-(4-chlorophenyl)-2-oxobutyl]phenyl]-1,2,4-triazine-3,5(2H,4H)-dione (interm. 69).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867207B2
Source datasetuspto-grants-2005_03
ORD IDord-44fb76121d9e4729a4a9475b1e117da5
Source noteuspto-grants-2005_03