HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270425Generated: November 1, 2026
Trimethyltin chloride → HCID 17983299, compound
https://huagongshe.com/reaction/1270425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 1,4-Benzodioxin | HCID 136071 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 17983299 | HCID 17983299 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202255B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-48a0d73502fb4fc1811bafe51fea8471 |
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| Source note | uspto-grants-2007_04 |
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