HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394180Generated: November 1, 2026
N-Methyl-4-nitroaniline → N,N,N'-trimethyl-N'-(4-nitrophenyl)-1,2-ethanediamine
https://huagongshe.com/reaction/1394180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyl-4-nitroaniline | HCID 7483 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N,N-Dimethylaminoethyl chloride hydrochloride | HCID 11636816 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N,N'-trimethyl-N'-(4-nitrophenyl)-1,2-ethanediamine | HCID 21873305 | 55.1% |
Reaction Steps
To a solution containing 1.52 g of 4-nitro-N-methylaniline (10 mmol) in 30 mL THF, was added 0.8 g of sodium hydride (60% dispension in oil, 20 mmol). After 5 minutes at room temperature, 2.59 g of 2-(dimethylamino)ethyl chloride hydrochloride (18 mmol) and 0.4 g of sodium hydride (60% dispension in oil, 10 mmol) were added. The reaction was heated at 60° C. for 5 hours. The solvent was concentrated in vacuo to yield a residue which was partitioned between ethyl acetate and 2 M sodium hydroxide solution. The organic phase was washed with water (3×), dried over anhydrous sodium sulphate, filtered, and concentrated in vacuo to yield the title compound as a brown oil (1.23 g, 55%). MS (ES+) m/e 224 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348339B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-7b824d5853984df1a2efee5aebc22edf |
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| Source note | uspto-grants-2008_03 |
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