HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580923Generated: October 25, 2026
4-(Chloromethyl)-2-nitroanisole → Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)
https://huagongshe.com/reaction/1580923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Chloromethyl)-2-nitroanisole | HCID 80785 | — |
| Reactant | Formamide, N,N'-[(methylimino)di-3,1-propanediyl]bis- | HCID 3084810 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1) | HCID 100848 | — |
Reaction Steps
A mixture of 54.0 parts of N,N-bis(3-formamidopropyl)methylamine, 50.4 parts of 4-methoxy-3-nitrobenzylchloride, and 78 parts of acetonitrile was stirred at reflux for seven and a half hours. An additional 78 parts of acetonitrile was added to the reaction mixture causing an oil to separate. Heating at reflux was continued for an additional two hours and the 140 parts of acetonitrile was distilled away and 200 parts of water was added. The remaining acetonitrile was removed by distillation and the cooled reaction mixture was filtered with the aid of diatomaceous earth to obtain an aqueous solution of N-methyl-N-(3-nitro-4-methoxybenzyl)-N,N-bis(3-formamidopropyl)ammonium chloride. The solution was used directly for reduction of the nitro group.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03935182 |
|---|
| Source dataset | uspto-grants-1976_01 |
|---|
| ORD ID | ord-82b97142c6844cd6a9ed5843d4a32c21 |
|---|
| Source note | uspto-grants-1976_01 |
|---|