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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 2-Chloroethylamine | HCID 13369 | — |
| Reactant | Bis(2-chloroethyl)-4-isocyanatophenylamine | HCID 10777647 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-[p-bis(beta-chloroethyl)aminophenyl]-N'-(beta'-chloroethyl)urea | HCID 15597311 | 86.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04803223 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-07a8cdab7d7e45a381cc72b5516a0644 |
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| Source note | uspto-grants-1989_02 |
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