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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433589Generated: November 3, 2026

Tetrahydrofuran → 2-Butyroylamino-4-(4-nitrophenoxy)pyridine

https://huagongshe.com/reaction/1433589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
Reactant4-(4-Nitrophenoxy)pyridin-2-amineHCID 22936716—
SolventWaterHCID 962—
Product2-Butyroylamino-4-(4-nitrophenoxy)pyridineHCID 22936677—

Reaction Steps

Butyroyl chloride (0.93 ml) was added dropwise to a stirred solution of 2-amino-4-(4-nitrophenoxy)pyridine (1.0 g), triethylamine (1.8 ml) and tetrahydrofuran (20 ml) at room temperature. After stirring for 1 hour, water was added, extraction was performed with ethyl acetate, the extract was dried over magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=2:1) to obtain 0.6 g of the target substance as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-d04a42bf09534488ad8382976a3d4a7f
Source noteuspto-grants-2009_11