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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374921Generated: October 30, 2026

Tetrabutylammonium Fluoride → 2-(5-ethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramide

https://huagongshe.com/reaction/1374921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-(5-trimethylsilylethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramideHCID 21078401—
ReactantDiethylether hexaneHCID 21584099—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(5-ethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramideHCID 21078398—

Reaction Steps

The product from Stage 1 (0.4 g) was dissolved in dichloromethane (10 ml) with stirring and a solution of tetra n-butylammonium fluoride in tetrahydrofuran (1.4 ml, 1M) was added. The mixture was stirred at ambient temperature for 2 hours then stored for 18 hours. Further dichloromethane was added and the organic phase was washed with water (twice), dried over magnesium sulphate and evaporated under reduced pressure to give a gum that was fractionated by chromatography (silica; diethyl ether/hexane, 2:1 by volume) to give the required product, 0.21 g, as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166621B2
Source datasetuspto-grants-2007_01
ORD IDord-6ec130d766524b81ba413f0c3c23ed0b
Source noteuspto-grants-2007_01