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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthylamine hydrochlorideHCID 11198—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(3-Nitrophenyl)propan-2-oneHCID 12507934—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-(1-Methyl-2-(3-nitrophenyl)ethyl]ethylamine hydrochlorideHCID 6020509785%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319920B1
Source datasetuspto-grants-2001_11
ORD IDord-23c4c77be53b40cbab5dcfa096471b31
Source noteuspto-grants-2001_11