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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | Phosphoramidic acid, ion(2-) | HCID 211207 | — |
| Reactant | Diethyl amino(phenyl)methylphosphonate | HCID 419299 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | alpha-[N-(2-chloroethyl)ureido]benzylphosphonic acid diethyl ester | HCID 53798997 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04567169 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-0cf852b59ea6435d8966c57c256c5a66 |
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| Source note | uspto-grants-1986_01 |
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