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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285324Generated: November 1, 2026

2-Chloroethyl isocyanate → alpha-[N-(2-chloroethyl)ureido]benzylphosphonic acid diethyl ester

https://huagongshe.com/reaction/1285324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl isocyanateHCID 16035—
ReactantPhosphoramidic acid, ion(2-)HCID 211207—
ReactantDiethyl amino(phenyl)methylphosphonateHCID 419299—
SolventChloroformHCID 6212—
Productalpha-[N-(2-chloroethyl)ureido]benzylphosphonic acid diethyl esterHCID 5379899785%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 0.05 mol of α-aminobenzylphosphonic acid diethyl ester in 30 ml of chloroform is cooled to 0° C. in an ice-bath and then a large excess (0.06 mol) of β-chloroethyl isocyanate is added. The temperature of the reaction is then maintained at 10° C. while continuing stirring until the reaction is complete. (Examination by thin layer chromatography is used to ascertain that the starting aminophosphonate has disappeared completely. After evaporation of the solvent under reduced pressure, the crystalline residue is taken up in ether and filtered, yielding 14.8 g of crystals. Yield: 85%; m.p.=82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567169
Source datasetuspto-grants-1986_01
ORD IDord-0cf852b59ea6435d8966c57c256c5a66
Source noteuspto-grants-1986_01