HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648469Generated: October 30, 2026
Tributyltin Chloride → 2-(Tributylstannyl)-3-thienyl-1,3-dioxolane
https://huagongshe.com/reaction/1648469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-(3-Thienyl)-1,3-dioxolane | HCID 315630 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Tributylstannyl)-3-thienyl-1,3-dioxolane | HCID 11134058 | 76.8% |
Reaction Steps
To a stirred solution of 15.6 g of 2-(3-thienyl)-1,3-dioxolane in 100 ml of anhydrous ether is added dropwise 74.3 ml of 1.48 N n-butyllithium under nitrogen at room temperature. After 15 minutes at reflux, the reaction mixture is cooled to -78° C. and 34.18 g of tri-n-butyltin chloride in 100 ml of dry tetrahydrofuran is added dropwise. After the addition is complete, the mixture is warmed to room temperature and the solvent is evaporated in vacuo to an oily residue. To the residue is added 100 ml of hexane and the resulting precipitate of lithium chloride collected. The filtrate is concentrated in vacuo to a residue which is distilled at 160°/0.04 mm Hg to give 34.16 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436333 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-0258e55da0f34fc1aef8b10787da227a |
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| Source note | uspto-grants-1995_07 |
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