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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700913Generated: October 29, 2026

Ethyl 4-oxobutanoate → 4-[N-Dodecyl-N-[2-[4-(3,3-Dimethoxy-4,4,4-trifluorobut-1-yl)phenoxy]ethyl]amino]butanoic acid, ethyl ester

https://huagongshe.com/reaction/1700913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-oxobutanoateHCID 82395—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-[2-[4-(3,3-Dimethoxy-4,4,4-trifluorobut-1-yl)phenoxy]ethyl]dodecylamineHCID 18319017—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product4-[N-Dodecyl-N-[2-[4-(3,3-Dimethoxy-4,4,4-trifluorobut-1-yl)phenoxy]ethyl]amino]butanoic acid, ethyl esterHCID 8675713273%

Reaction Conditions

Temperature22 °C

Reaction Steps

A solution of N-[2-[4-(3,3-dimethoxy-4,4,4-trifluorobut-1-yl)phenoxy]ethyl]dodecanamine (2.0 g, 4.2 mmol) in methanol (50 ml) was treated with sodium cyanoborohydride (0.55 g, 8.4 mmol) and ethyl 4-oxobutyrate (1.04 g, 8.4 mmol). The resulting mixture was stirred at 22° C. for 16 h, diluted with diethyl ether (350 ml), washed with water (200 ml), brine (200 ml), dried over magnesium sulfate and concentrated in vacuo. The residue was chromatographed on silica gel (hexane/AcOEt 9:1 to 6:1) to afford the title compound (1.8 g, 73%) as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-4c84a64cad434dde887d63bb071dab5c
Source noteuspto-grants-2002_02