HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366860Generated: October 31, 2026
Tributyltin Chloride → HCID 23290213, compound
https://huagongshe.com/reaction/366860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | HCID 10692157 | HCID 10692157 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23290213 | HCID 23290213 | 99% |
Reaction Steps
n-Butyllithium (1.8 mL, 4.5 mmol, 2.5 M solution in hexane) was added dropwise at -78° C. to a solution of 3,4-didecyloxythiophene (1.86 g, 4.69 mmol) in anhydrous THF (200 mL) under nitrogen. The solution was stirred for 1 h and warmed to -40° C. Tributylstannyl chloride (1.47 g, 4.52 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-didecyloxythiophene, obtained as a light yellow liquid, yield=99%. MS(EI) m/z (rel int): 629 [(M)+ --C4H9, 22%], 396 [(M+ --C12H27Sn), 8.5%], 256 [(M+ --C22H47Sn), 3%] and 116 [(M+ --C32H67Sn), 43%].
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-73733c3a78f24f87986409ba0a0d89ec |
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| Source note | uspto-grants-2000_10 |
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