Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071500Generated: October 26, 2026

Water → 1-(2,5-Dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea

https://huagongshe.com/reaction/2071500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBenzene, 1,4-dichloro-2-isocyanato-HCID 79360—
Reactant1-Methylpyrrolidin-2-imine hydrochlorideHCID 12448967—
SolventBenzeneHCID 241—
Product1-(2,5-Dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)ureaHCID 54230281—

Reaction Steps

To 6.73 g. (0.05 mole) of 1-methyl-2-iminopyrrolidine HCl is added 1 ml. of water and 50 ml. of benzene. After solution is complete (magnetic stirring), 10 ml. of aqueous sodium hydroxide (50%) is added in one portion. After stirring for about 1 min., the benzene layer is decanted onto anhydrous potassium carbonate. The extraction is repeated twice. After drying (occasional swirling) the combined benzene extracts are filtered (dicalite) from drying agent and 9.4 g. (0.05 mole) of 2,5-dichlorophenylisocyanate is added to the filtrate in one portion with swirling. After stirring for 3 hours, the solvent is removed in vacuo affording a colorless solid, 1-(2,5-dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea. Recrystallization from acetone (twice) yields the pure product, m.p. = 148.5°-150.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046909
Source datasetuspto-grants-1977_09
ORD IDord-4abd23e35fd1426ea75e859d24fda9f4
Source noteuspto-grants-1977_09