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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868307Generated: October 30, 2026

Hydrochloric Acid → HCID 131714993, compound

https://huagongshe.com/reaction/868307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-CyanoacetylethylcarbamateHCID 23112—
ReactantSodium AcetateHCID 517045—
ReactantHCID 21288227HCID 21288227—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 131714993HCID 13171499374.1%

Reaction Steps

To a stirred and cooled (5°-10° C.) mixture of 15.2 parts of 4-amino-2-chloro-α-(4-chlorophenyl)-α,5-dimethylbenzeneacetonitrile, 14.4 parts of concentrate hydrochloric acid and 125 parts of acetic acid was added dropwise, during a 30 minutes period, a solution of 3.5 parts of sodium nitrite in 15 parts of water at about 10° C. Upon completion, the whole was stirred for 30 minutes and then 10 parts of sodium acetate and 7.8 parts of ethyl (2-cyanoacetyl)carbamate were added, during a period of 2 hours, at room temperature. The reaction mixture was poured into 500 parts of water. The product was filtered off, washed with water and dissolved in dichloromethane. The organic layer was dried, filtered and evaporated. The residue was 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 the eluent was evaporated in vacuo. The residue was stirred in 2-propanol. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 17.5 parts (74.1%) of ethyl[2-[[5-chloro-4-[1-(4-chlorophenyl)-1-cyanoethyl]-2-methylphenyl]hydrazono]-2-cyanoacetyl]carbamate (intermediate 44).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778887
Source datasetuspto-grants-1988_10
ORD IDord-f464a9ea90ef4fd7b4d0c7b8de9056bc
Source noteuspto-grants-1988_10