HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79972Generated: October 26, 2026
Hexane → 2,6-Bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b']dithiophene
https://huagongshe.com/reaction/79972
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Benzo[1,2-b:4,5-b']dithiophene | HCID 11106168 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b']dithiophene | HCID 58545582 | 42% |
Reaction Steps
To a stirred solution of benzo[1,2-b:4,5-b′]dithiophene (820 mg, 4.3 mmol) in THF (100 mL) under argon at −78° C. was added a solution of n-butyllithium (2.5 M, 3.44 mL, 8.6 mmol). The solution was stirred at −78° C. for 30 minutes and then warmed to −20° C. for 30 minutes. Tri-n-butyltin chloride (2.34 mL, 8.6 mmol) was added and the reaction mixture was stirred at −20° C. for 30 minutes and then allowed to warm to room temperature. After 16 hours, hexane was added and the reaction was successively washed with water and brine, dried (MgSO4), concentrated and purified by flash chromatography (100% hexanes). 2,6-bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b′]dithiophene (1.4 g, 42%) was isolated along with product contaminated with the monostannylated benzodithiophene. 1H-NMR: 400 MHz, (CDCl3) δ: 8.27 (s, 2H), 7.38 (s, 2H), 1.65-1.57 (m, 12H), 1.41-1.32 (m, 12H), 1.26-1.11 (m, 12H), 0.91 (t, J=7.3 Hz, 18H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841278B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f4bb72d0c4af46c5a6604ce826a41e6d |
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| Source note | uspto-grants-2014_09 |
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