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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279281Generated: October 31, 2026

Water → HCID 18427791, compound

https://huagongshe.com/reaction/1279281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanoacetic acidHCID 9740—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant(2,4,6-Trichlorophenyl)hydrazineHCID 79234—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 18427791HCID 18427791—

Reaction Steps

Cyanoacetic acid (8.5 g, 0.10 mol) in 200 mL of dry ether was treated with 20.8 g (0.10 mol) of phosphorous pentachloride, warmed briefly to reflux and let cool to room temperature at which time all of the phosphorous pentachloride, had dissolved. After a small amount of insoluble material was removed by filtration, the ether was removed on the rotary evaporator. Then 100 mL of toluene was added and stripped to remove phosphorous oxytrichloride. The residual pale yellow oil was immediately dissolved in 50 mL of cold methylene dichloride and added to a cold suspension of 21.15 g (0.10 mol) of 2,4,6-trichlorophenylhydrazine in 14.0 mL of triethylamine and 100 mL of methylene dichloride, keeping the temperature below 20° C. by use of an ice bath. The reaction mixture was allowed to warm to room temperature and stirred for one hour. Then 500 mL of cold water was added. The precipitated solid was filtered and washed with water and with a little methylene dichloride to give the intermediate 2-cyano-N-(2,4,6-trichlorophenyl)acethydrazide, 14.92 g (54%), m.p. 166-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448265B1
Source datasetuspto-grants-2002_09
ORD IDord-52663fe73d8f435ebd8c9c27ce9e67a8
Source noteuspto-grants-2002_09