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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071517Generated: November 1, 2026

Benzene, 1-chloro-3-isocyanato- → HCID 3039369, compound

https://huagongshe.com/reaction/2071517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-chloro-3-isocyanato-HCID 17968—
ReactantHCID 12449021HCID 12449021—
SolventBenzeneHCID 241—
ProductHCID 3039369HCID 3039369—

Reaction Steps

The hydrochloride salt of 1-ethyl-2-iminopyrrolidine (7.43 g.; 0.05 mole) is converted to free base (5.6 g.; 0.05 mole) by adding 7 ml. of 50% NaOH to an aqueous slurry (minimal amount of water) of the salt and benzene extraction. After drying over K2CO3, the benzene solution is stirred at room temperature and 7.68 g. (0.05 mole) of m-chlorophenylisocyanate, dissolved in anhydrous benzene, is added. The reaction mixture is stirred for 13/4 hours and the solvent is then evaporated in vacuo leaving a solid residue, 1-m-chlorophenyl-3-(1-ethyl-2-pyrrolidylidene)urea. Recrystallizations from ethyl acetate yields the pure product, m.p. = 122°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046909
Source datasetuspto-grants-1977_09
ORD IDord-2b84f34400174c4c95544fb530bed912
Source noteuspto-grants-1977_09