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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271485Generated: November 2, 2026

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

https://huagongshe.com/reaction/1271485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactantbeta-nitrostyrene, (E)-HCID 5284459—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-[(2-amino-1-phenylethyl)amino]propanoateHCID 18451931148.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

trans-β-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 (12M; 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 numberUS07205292B2
Source datasetuspto-grants-2007_04
ORD IDord-1e44049847a14d4caead57f5d2cb5520
Source noteuspto-grants-2007_04