Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19405Generated: October 26, 2026

Ethyl 2-(diphenylmethyleneamino)acetate → (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester

https://huagongshe.com/reaction/19405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
Reactant(S)-(+)-1-Iodo-2-methylbutaneHCID 5702528—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl esterHCID 8663524474%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (benzhydrylidene-amino)-acetic acid ethyl ester (5.48 g, 20.5 mmol) in tetrahydrofuran (40 mL) was treated with potassium t-butoxide (2.83 g, 25.26 mmol) and stirred at 0° C. for 35 min. At this time a solution of (S)-1-iodo-2-methyl-butane (5.00 g, 25.25 mmol) in tetrahydrofuran (20 mL) was added via syringe and the resulting solution stirred at 0° C. for 10 min and then room temperature overnight. The reaction mixture was concentrated in vacuo and the residue partitioned between diethyl ether and dilute aqueous hydrochloric acid. The layers were separated, and the organic layer was washed with brine and concentrated in vacuo. The residue was purified by ISCO flash chromatography (RediSep silica 120 g, 0% to 10% ethyl acetate/hexanes) which afforded (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester (5.09 g, 74%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-e2b1e4a3f0e64d58bf4a398c4d0d1a9d
Source noteuspto-grants-2010_06