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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061675Generated: November 3, 2026

Hydrochloric Acid → Ethyl 2-amino-4-methoxybutanoate hydrochloride

https://huagongshe.com/reaction/1061675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-amino-4-methoxybutanoate hydrochlorideHCID 86759889—

Reaction Steps

Sodium hydride (1.8 g) is added to a solution of N-(diphenylmethylene)glycine ethyl ester in tetrahydrofuran under ice cooling, then the temperature is raised to room temperature, and the mixture is stirred for one hour. 2-Bromoethyl methyl ether (4.22 ml) is added to the mixture, and the whole is refluxed overnight. The reaction mixture is cooled to room temperature, 0.1 N hydrochloric acid is added thereto, and the whole is stirred for four hours. Ethyl acetate is added to the reaction mixture, and the whole is extracted with 0.1 N hydrochloric acid. The extract is basified with a saturated aqueous sodium hydrogencarbonate solution, and the whole is extracted with ethyl acetate. The extract is washed with saturated brine and dried over anhydrous magnesium sulfate. The extract is concentrated under reduced pressure, a 4 N hydrogen chloride/ethyl acetate solution is added to the resulting residue, and the whole is concentrated under reduced pressure again to give the titled reference compound (2.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960575B2
Source datasetuspto-grants-2005_11
ORD IDord-1264bdd737ce4ff1bc00306a35d44854
Source noteuspto-grants-2005_11