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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980567Generated: October 31, 2026

2-Chlorobenzoyl isocyanate → 1-(2-Chlorobenzoyl)-3-[2,5-dimethyl-3-chloro-4-(2-chloro-4-phenylphenoxy) phenyl]urea

https://huagongshe.com/reaction/980567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl isocyanateHCID 9942311—
Reactant4-(2-Chloro-4-phenylphenoxy)-2,5-dimethyl-3-chloroanilineHCID 13772929—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product1-(2-Chlorobenzoyl)-3-[2,5-dimethyl-3-chloro-4-(2-chloro-4-phenylphenoxy) phenyl]ureaHCID 13772930—

Reaction Steps

To a solution containing 1.61 grams (0.004 moles) of 4-(2-chloro-4-phenylphenoxy)-2,5-dimethyl-3-chloroaniline prepared in Part B and 3 milliliters of toluene, which solution was warmed to 40° C.-50° C. and placed under an atmosphere of nitrogen, was added a solution containing 0.98 grams (0.005 moles) of 2-chlorobenzoyl isocyanate and 0.05 milliliters of toluene. The resulting mixture was then heated to a temperature of 60° C.-70° C, for a period of 0.5-1.0 hours. After cooling to ambient temperature, the reaction mixture was diluted with 4 milliliters of toluene and 2 milliliters of hexane. This mixture was then filtred to give a solid material. The solid material was washed once with a toluene-hexane mixture (1:2 volume ratio) and finally once with hexane and then dried overnight in a vaccum oven at 50° C. This afforded a tan powder material having a melting point of 198° C.-199° C. Elemental analysis of the tan powder indicated the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638088
Source datasetuspto-grants-1987_01
ORD IDord-dab7383a53d74a53ae2023c93ef92d64
Source noteuspto-grants-1987_01