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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381571Generated: October 31, 2026

Hydrochloric Acid → N-[p-bis(beta-chloroethyl)aminophenyl]-N'-(beta'-chloroethyl)urea

https://huagongshe.com/reaction/1381571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTributylamineHCID 7622—
Reactant2-ChloroethylamineHCID 13369—
ReactantBis(2-chloroethyl)-4-isocyanatophenylamineHCID 10777647—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductN-[p-bis(beta-chloroethyl)aminophenyl]-N'-(beta'-chloroethyl)ureaHCID 1559731186.3%

Reaction Conditions

Temperature34 °C

Reaction Steps

A mixture of β-chloroethylamine.HCl (5.80 g, 0.05 mole), hexane (60 ml), N,N-dimethylformamide (30 ml) and tributylamine (14.83 g; 0.08 mole) was cooled to -10° C., and an ether solution (100 ml) of p-bis(β-chloroethyl)aminophenyl isocyanate (12.9 g; 0.05 mole) was added with stirring. One hour later, the reaction mixture was heated at 34° C. for 6 hours. Low-boiling fractions were removed by distillation under reduced pressure. The residue was poured into ice water (500 ml), and the resulting white solid was collected by filtration and dried to give N-[p-bis(β-chloroethyl)aminophenyl]-N'-(β'-chloroethyl)urea (14.61 g). The yield was 86.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803223
Source datasetuspto-grants-1989_02
ORD IDord-07a8cdab7d7e45a381cc72b5516a0644
Source noteuspto-grants-1989_02