Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N,N-Bis(2-chloroethyl)-3-nitrobenzenamine | HCID 32679 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22096854 | HCID 22096854 | 192.1% |
Reaction Steps
3-[N,N-Bis(2-chloroethyl)amino]nitrobenzene (2.0 g; 7.6 mmol) was dissolved in 35 ml of concentrated hydrochloric acid, followed by the addition of 6.9 g (30.6 mmol; 4.0 equivalents) of tin(II) chloride dihydrate. The resultant mixture was stirred under heat for 1 hour over an oil bath controlled at 100° C. The reaction mixture was allowed to cool down to room temperature, followed by dilution with water. The diluted solution was basified with concentrated aqueous ammonia and then extracted twice with ethyl acetate. The extract was dried over sodium sulfate and then concentrated under reduced pressure. The residue so obtained was added with 4N hydrochloric acid/dioxane and concentrated. The concentrate was then crystallized from a small amount of methanol/ether, whereby 1.97 g (7.3 mmol) of the title compound were obtained as yellow crystals (yield: 96.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05852011 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-8e51c7e470e24bd18e4465f3228bec2f |
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| Source note | uspto-grants-1998_12 |
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