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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355360Generated: October 30, 2026

Hydrochloric Acid → HCID 131720911, compound

https://huagongshe.com/reaction/355360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-CyanoacetylethylcarbamateHCID 23112—
ReactantSodium AcetateHCID 517045—
Reactant(4-Amino-2,6-dichlorophenyl)(4-chlorophenyl)acetonitrileHCID 15068435—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 131720911HCID 131720911—

Reaction Steps

To a stirred and cooled (5-10 degrees C) mixture of 15.2 parts of 4-amino-2,6-dichloro-α-(4-chlorophenyl)-benzeneacetonitrile (intermediate 2), 14.4 parts of concentrate hydrochloric acid and 125 parts of acetic acid is added dropwise, during a 30 minutes period, a solution of 3.5 parts of sodium nitrite in 15 parts of water at about 10 degrees C. Upon completion, the whole is stirred for 30 minutes and then 10 parts of sodium acetate and 7.8 parts of ethyl(2-cyanoacetyl)carbamate are added, during a period of 2 hours, at room temperature. The reaction mixture is poured into 500 parts of water. The product is filtered off, washed with water and dissolved in dichloromethane. The organic layer is dried, filtered and evaporated. The residue is purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated in vacuo. The residue is stirred in 2-propanol. The product is filtered off, washed with 2,2'-oxybispropane and dried, yielding ethyl[2-[[3,5-dichloro-4-[(4-chlorophenyl)cyanomethyl]phenyl]hydrazono]-2-cyanoacetyl]carbamate (intermediate 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05830893
Source datasetuspto-grants-1998_11
ORD IDord-0d95f4f2b70444fb9f1b10efe3ac07a5
Source noteuspto-grants-1998_11