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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488745Generated: October 30, 2026

Triethylamine → (S)-2-(4-fluoro-benzylamino)-propionic acid methyl ester

https://huagongshe.com/reaction/488745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product(S)-2-(4-fluoro-benzylamino)-propionic acid methyl esterHCID 4323025091%

Reaction Steps

To a solution of (S)-2-amino-propionic acid methyl ester hydrochloride (25 g, 179 mmol) and 4-fluorobenzaldehyde (23 mL, 215 mmol) in 1,2-dichloroethane (200 mL) was added triethylamine (25 mL, 179 mmol). The resulting mixture was stirred for two hours at ambient temperature followed by addition of sodium triacetoxyborohydride (57 g, 268 mmol) in four portions. The resulting mixture was stirred overnight at ambient temperature. The reaction was neutralized with dilute aqueous sodium hydroxide solution and extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel gave the title compound (34.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974817B2
Source datasetuspto-grants-2005_12
ORD IDord-780236a5cbb549a4823ab7cf03afa5af
Source noteuspto-grants-2005_12