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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642962Generated: October 27, 2026

Water → N-Methyl-N-{2-[(tributylstannyl)methoxy]ethyl}cyclohexaneamine

https://huagongshe.com/reaction/642962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-(Cyclohexylmethylamino)ethanolHCID 277582—
ReactantTributyl(iodomethyl)stannaneHCID 10862926—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Methyl-N-{2-[(tributylstannyl)methoxy]ethyl}cyclohexaneamineHCID 5925971986%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of sodium hydride (50%, 241 mg, 5.0 mmol) and tetrahydrofuran (20 ml) was added 2-[cyclohexyl(methyl)amino]ethanol (791 mg, 5.0 mmol) at 0° C. (external temperature). Then, the reaction mixture was stirred at 60° C. for 30 minutes. After the reaction mixture was cooled at 0° C. (external temperature), to the reaction mixture was added dropwise a solution of tributyl-iodomethyl-tin (2.2 g, 5.0 mmol) in tetrahydrofuran (5 ml), and the reaction mixture was stirred at 60° C. for 1 hour. After the reaction mixture was cooled at room temperature (external temperature), water was added to stop the reaction. Ethyl acetate was added to the reaction mixture, and the organic layer was separated. After the organic layer was washed with water, an aqueous saturated sodium chloride solution, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (heptane:ethyl acetate=20:1, NH silica gel) to obtain the title compound (790.7 mg, 4.3 mmol, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696347B2
Source datasetuspto-grants-2010_04
ORD IDord-210dbaacbcd64b4dbdd1bdd888419e6a
Source noteuspto-grants-2010_04