HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399513Generated: November 1, 2026
N,N-Bis(2-chloroethyl)-3-nitrobenzenamine → HCID 22096854, compound
https://huagongshe.com/reaction/399513
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Bis(2-chloroethyl)-3-nitrobenzenamine | HCID 32679 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22096854 | HCID 22096854 | 192.1% |
Reaction Steps
In 35 ml of concentrated hydrochloric acid was dissolved 2.0 g (7.6 mmols) of 3-[N,N-bis(2-chloroethyl)amino]nitrobenzene, and 6.9 g (30.6 mmols, 4.0 eq.) of stannic chloride (II) dihydrate was added, followed by stirring for 1 hour in an oil bath at 100° C. Next, the solution was allowed to stand until its temperature lowered to room temperature, and then diluted with water. The solution was basified with concentrated ammonia water, extracted with ethyl acetate twice, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. Afterward, 4N hydrochloric acid and dioxane were added to the resulting residue, and after concentration, the residue was crystallized from a small amount of methanol-ether to obtain 1.97 g (7.3 mmols, 96.1%) of the desired compound in the state of yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05821258 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-7f95ec6f1908402e9f97561588d3b7d0 |
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| Source note | uspto-grants-1998_10 |
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