HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257981Generated: October 26, 2026
Hexane → 5-Trimethylstannyl-4,4'-didodecyl-2,2'-bithiophene
https://huagongshe.com/reaction/1257981
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 5-Bromo-4,4'-didodecyl-2,2'-bithiophene | HCID 67120820 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Trimethylstannyl-4,4'-didodecyl-2,2'-bithiophene | HCID 57572693 | 90% |
Reaction Steps
To a solution of 5-bromo-4,4′-didodecyl-2,2′-bithiophene (29A, 100 mg, 0.172 mmol) in 4.0 mL of THF was added dropwise a solution of n-butyllithium in hexane (0.076 mL, 2.5 M, 0.189 mmol) at −78° C. The solution was stirred at −78° C. for 1 hour and a solution of trimethyltin chloride in THF (0.20 mL, 1.0 M, 0.20 mmol) was added in one portion. The solution was warmed to room temperature and 10.0 mL of water and 10.0 mL of diethylether were added. The organic layer was separated and washed twice with 20 mL of water and dried over magnesium sulfate. After filtration, the filtrate was concentrated in vacuo to yield 5-trimethylstannyl-4,4′-didodecyl-2,2′-bithiophene (29, 0.103 g, 90% yield) as a yellow oil. 1H NMR (CDCl3): δ 0.84-1.64 (m, 46H), 2.58 (m, 4H), 6.77 (s, 1H), 6.99 (s, 1H), 7.13 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE044304E1 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-cb0ead2b64da435eb05658c051c743c5 |
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| Source note | uspto-grants-2013_06 |
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