HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721313Generated: October 28, 2026
Nitrogen mustard hydrochloride → HCID 673952, compound
https://huagongshe.com/reaction/1721313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen mustard hydrochloride | HCID 5935 | — |
| Reactant | 2-Chloro-5-nitroaniline | HCID 22691 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 673952 | HCID 673952 | 66.5% |
Reaction Steps
A mixture of 2-chloro-5-nitrobenzenamine (7.95 g) and 2-chloro-N-(2-chloroethyl)-N-methylethanamine hydrochloride (8.86 g) in chlorobenzene (40 ml) under nitrogen was heated to reflux for 3 days before cooling and diluting with dichloromethane (60 ml). The reaction mixture was then extracted with water (2×500 ml), the aqueous layers combined and basified with 2N sodium hydroxide, then extracted with dichloromethane (4×400 ml). The combined, dried extracts were concentrated in vacuo to give a dark brown oil (7.82 g) which was purified by FCC eluting with ether to give a dark brown oil which crystallised upon standing. The material was dissolved in ethanol (40 ml) and boiled up with some charcoal (300 mg). The hot ethanolic suspension was filtered and concentrated in vacuo to give the title compound as a yellow oil which crystallised on standing (5.25 g) m.p.63°-64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05510350 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-56bf79923679473ab27778839e8a6a49 |
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| Source note | uspto-grants-1996_04 |
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