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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973943Generated: November 2, 2026

2,4,6-Trichlorophenyl Isocyanate → HCID 54537487, compound

https://huagongshe.com/reaction/1973943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trichlorophenyl IsocyanateHCID 613574—
Reactant1-Methyl-2-pyrrolidinimineHCID 12448966—
SolventBenzeneHCID 241—
ProductHCID 54537487HCID 54537487—

Reaction Steps

The hydrochloride salt of 2-imino-1-methylpyrrolidine (5.52 g., 0.041 mole) is converted to free base in benzene in the usual manner. Then 9.08 g. (0.041 mole) of 2,4,6-trichlorophenylisocyanate [made according to the method of K. Inukai and Y. Maki, Kogyo Kagaku Zasshi, 70 (4), 491-4 (1967)] dissolved in anhydrous benzene is added with stirring. The reaction mixture is stirred for 2 hours and the solvent is evaporated in vacuo to give a solid residue of 1-(2,4,6-trichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea. Recrystallizations from ethyl acetate yields the pure product, m.p. = 160°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998958
Source datasetuspto-grants-1976_12
ORD IDord-44ecc106d0c94015a02f996520a41d7e
Source noteuspto-grants-1976_12