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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383910Generated: November 2, 2026

Ethyl 4-oxobutanoate → 4-[N-dodecyl-N-2-[4-iodophenoxy]ethylamino]butanoic acid, ethyl ester

https://huagongshe.com/reaction/1383910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-oxobutanoateHCID 82395—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-2-[4-Iodophenoxy]ethyldodecylamineHCID 18319005—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-[N-dodecyl-N-2-[4-iodophenoxy]ethylamino]butanoic acid, ethyl esterHCID 8675712089%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a mixture of N-2-[4-iodophenoxy]ethyldodecylamine ( 4.0 g, 9.3 mmol) and sodium cyanoborohydride (1.45 g, 23 mmol) in methanol (80 ml) was added dropwise a solution of ethyl 4-oxobutyrate (Fournet, G. ; Balme, G.; Barieux, J. J. and Gore, J. Tetrahedron, 1988, 44, 5821) (2.4 g, 18 mmol) in methanol (20 ml) over a period of 10 min. The resulting mixture was stirred at 22° C. for 24 h, and then diluted with ethyl acetate (600 ml), washed with brine (3×250 ml). The aqueous phase was extracted with ethyl acetate (150 ml), and the combined organic layers were dried over sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica gel (Hexane/ethyl acetate 8:1 to 6:1) to afford the title compound (4.5 g, 89%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255496B1
Source datasetuspto-grants-2001_07
ORD IDord-e5fea5b26ca14b5caae909f62ed46e01
Source noteuspto-grants-2001_07