HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429816Generated: October 30, 2026
Hydrochloric Acid → 2-(1-Methyl-2-(3-nitrophenyl)ethyl]ethylamine hydrochloride
https://huagongshe.com/reaction/429816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-(3-Nitrophenyl)propan-2-one | HCID 12507934 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Methyl-2-(3-nitrophenyl)ethyl]ethylamine hydrochloride | HCID 60205097 | 85% |
Reaction Steps
In dichloromethane (50 ml) was combined 1-(3-nitrophenyl)propan-2-one (1.44 grams, 8 mmole), ethylamine hydrochloride (0.42 grams, 8 mmole), and triethylamine (1.1 ml, 11 mmole). The mixture was stirred under nitrogen at room temperature for 30 minutes. Then sodium triacetoxyborohydride (2.5 grams, 11.7 mmole) was added in one portion. The mixture was stirred under nitrogen 18 hours. Additional ethylamine hydrochloride (0.4 grams) was added. After another 18 hours the mixture was diluted with ethyl ether, washed with 10% sodium hydroxide solution (50 ml), dried over anhydrous magnesium sulfate and the solvent removed under vacuum to give an oil. This oil was taken up into methanol, acidified with 1M hydrochloric acid in ether and the salt was precipitated by further addition of ether. The resulting solid was filtered and air dried to give [2-(1-methyl-2-(3-nitrophenyl)ethyl]ethylamine hydrochloride (1.4 grams, 85%), m.p. 173-175° C., M+H 208.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319920B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-23c4c77be53b40cbab5dcfa096471b31 |
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| Source note | uspto-grants-2001_11 |
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