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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270425Generated: November 1, 2026

Trimethyltin chloride → HCID 17983299, compound

https://huagongshe.com/reaction/1270425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyltin chlorideHCID 14016—
Reactant1,4-BenzodioxinHCID 136071—
ReactantPotassium FluorideHCID 522689—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 17983299HCID 17983299—

Reaction Conditions

Temperature-78 °C

Reaction Steps

14.91 mmol of 1,4-benzodioxine are dissolved in 18 ml of anhydrous tetrahydrofuran under an anhydrous atmosphere, and the temperature of the solution is lowered to −78° C. 23.86 mmol of a 1.5M solution of n-butyllithium in hexane are added dropwise to the reaction mixture, which is stirred at −78° C. for 2 hours 15 minutes. 37.28 mmol of trimethyltin chloride dissolved in 10 ml of anhydrous tetrahydrofuran are added dropwise and the reaction mixture is stirred at −78° C. for 45 minutes and then returned to ambient temperature for 15 hours. The reaction mixture is hydrolysed with 15% aqueous potassium fluoride solution and is stirred for 45 minutes. The precipitated tin salts are removed by filtration, and the aqueous phase is extracted 3 times with ethyl acetate. The organic phases are combined and concentrated. Purification by flash chromatography over silica gel (petroleum ether/ethyl acetate: 95/5) allows the expected product to be obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202255B2
Source datasetuspto-grants-2007_04
ORD IDord-48a0d73502fb4fc1811bafe51fea8471
Source noteuspto-grants-2007_04