HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355871Generated: October 27, 2026
Tributyltin Chloride → 2-(Tributylstannyl)-3-thienyl-1,3-dioxolane
https://huagongshe.com/reaction/355871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-(3-Thienyl)-1,3-dioxolane | HCID 315630 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Butyllithium | HCID 178418339 | — |
| Product | 2-(Tributylstannyl)-3-thienyl-1,3-dioxolane | HCID 11134058 | 77% |
Reaction Steps
To a stirred solution of 15.6 g (0.10 mol) of 2-(3-thienyl)-1,3-dioxolane in 100 ml of anhydrous ether, n-butyl-lithium (1.48N, in hexane, 74.3 ml) is added dropwise under nitrogen at room temperature. After being refluxed for 15 minutes, the reaction mixture is cooled to -78° C. and tri-n-butyltin chloride (34.18 g, 0.105 mol) in 100 ml of dry tetrahydrofuran is added dropwise. After the addition is complete, the mixture is warmed to room temperature and the solvent evaporated. To the oily residue 100 ml of hexane is added, and the resulting precipitate (LiCl) is filtered off. The filtrate is evaporated and the residue distilled at reduced pressure, giving 34.16 g (77%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834461 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-16b11d67575b4ea09809fadeb3d31e9d |
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| Source note | uspto-grants-1998_11 |
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