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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383931Generated: November 2, 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/1383931

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 numberUS06255496B1
Source datasetuspto-grants-2001_07
ORD IDord-c3cd23191cc448b5a702e36209016de8
Source noteuspto-grants-2001_07