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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642959Generated: October 30, 2026

Tetrahydrofuran → HCID 59259720, compound

https://huagongshe.com/reaction/642959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-(2-Hydroxyethyl)-4-methylpiperazineHCID 231184—
ReactantTributyl(iodomethyl)stannaneHCID 10862926—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59259720HCID 5925972092%

Reaction Steps

To a mixture of 1-(2-hydroxyethyl)-4-methylpiperazine (1.0 g, 6.9 mmol) and tetrahydrofuran (15 ml) was added sodium hydride (60%, 277 mg, 6.9 mmol) at 0° C. (external temperature), and the reaction mixture was stirred at room temperature for 30 minutes. Then, to the reaction mixture was added dropwise a mixture of tributyl-iodomethyl-tin (2.0 g, 4.6 mmol) and N,N-dimethylformamide (15 ml) at 0° C. (external temperature). Then, the reaction mixture was stirred at room temperature for 1.5 hours. To the reaction mixture were added water and ethyl acetate, and the organic layer was separated. The organic layer was washed with water and an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1, NH silica gel) to obtain the title compound (1.9 g, 4.2 mmol, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696347B2
Source datasetuspto-grants-2010_04
ORD IDord-3a1d4e123ddc4ad48ba511ec49e9014a
Source noteuspto-grants-2010_04