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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279548Generated: October 27, 2026

Ethyl 2-(diphenylmethyleneamino)acetate → Ethyl alpha-amino-3-methyl-5-oxopyrrolidine-2-pentanoate

https://huagongshe.com/reaction/1279548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
Reactant5-(3-Bromopropyl)-4-methylpyrrolidin-2-oneHCID 18428582—
ReactantSodiumbis(trimethylsilylamide)HCID 86599718—
SolventTetrahydrofuranHCID 8028—
ProductEthyl alpha-amino-3-methyl-5-oxopyrrolidine-2-pentanoateHCID 18428636—

Reaction Conditions

Temperature-72 °C

Reaction Steps

A solution of N-(diphenylmethylene)glycine ethyl ester (Aldrich, 37 mmol) in THF (20 mL) is added to −72° C. solution of sodium bis (trimethylsilylamide) (35 mmol, 0.5 M in THF), while the solution is kept below −65° C. The resulting solution is then stirred at −72° C. for 30 min.; followed by the rapid addition of a cooled solution (−72° C.) of the product from EXAMPLE 236 (24 mmol) in THF via canula. The cooling bath is removed immediately and the mixture allowed to warm to 0° C. for 4 h. The reaction mixture is partitioned between ether and 10% aqueous sodium bisulfate, then dried and concentrated. The product is purified by column chromatography. This intermediate is then treated with 0.1 N aqueous hydrochloric acid for 3 h, followed by extraction with ether and lyophilization of the aqueous solution, to yield the title material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448286B1
Source datasetuspto-grants-2002_09
ORD IDord-f4f1053b188a4bdf962cb363ccdc3d17
Source noteuspto-grants-2002_09