HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366859Generated: October 26, 2026
Tributyltin Chloride → Tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane
https://huagongshe.com/reaction/366859
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 3,4-Ethylenedioxythiophene | HCID 4421864 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane | HCID 15891053 | 98% |
Reaction Steps
n-Butyllithium (77 mL, 192.5 mmol, 2.5 M solution in hexane) was added dropwise at -78° C. to a solution of 3,4-(ethylenedioxy)thiophene (25 g, 175.9 mmol) in anhydrous THF (100 mL) under nitrogen. The solution was stirred for 1 h and warmed to -40° C. Tributylstannyl chloride (85.89 g, 263.9 mmol) was added and the entire solution was finally allowed to warm to room temperature. At room temperature the mixture was filtered using Celite and the solvent was stripped. The organo-tin compound was vacuum dried to give 2-(tributylstannyl)-3,4-(ethylenedioxy)thiophene, obtained as a dark yellow liquid, yield=98%. MS(EI) m/z (rel int): 375 [(M)+ --C4H8, 100%] and 319[(M)+ --C8H16, 18%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06130339 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-891cc2ba15b04d7b843f32e705f27aa2 |
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| Source note | uspto-grants-2000_10 |
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