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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725609Generated: November 3, 2026

Beta-Nitrostyrene → Ethyl 3-[(2-amino-1-phenylethyl)amino]propanoate

https://huagongshe.com/reaction/1725609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-NitrostyreneHCID 7626—
ReactantDiisopropylethylamineHCID 81531—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-[(2-amino-1-phenylethyl)amino]propanoateHCID 18451931148.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trans-□-Nitrostyrene (4.04 g, 27.1 mmol) was added to a solution of ethyl 3-aminopropanoate hydrochloride (4.16 g, 27.1 mmol), and N,N-diisopropylethylamine (9.43 mL, 54.2 mmol) in acetonitrile (70 mL). After 15 min, anhydrous hydrochloric acid gas was bubbled into the solution until acidic. The mixture was concentrated, redissolved in ethanol (60 mL) and aqueous hydrochloric acid (12 M; 30 mL), and cooled to 0° C. Zinc dust (8.80 g, 134 mmol) was added in portions over 5 min. After 0.5 h, the mixture was concentrated to remove ethanol and saturated aqueous sodium carbonate was added. The mixture was extracted with dichloromethane (3×), and the combined organic extracts were dried over magnesium sulfate, filtered and concentrated to give the title compound (9.5 g). MS 237 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491713B2
Source datasetuspto-grants-2009_02
ORD IDord-1c98881dc1db454bb19725d22035e607
Source noteuspto-grants-2009_02