HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1509353Erstellt: 25. Oktober 2026
Stannous Chloride → 4,8-Bis(2-ethylhexyl)benzo[1,2-b:4,5-b']dithiophene
https://huagongshe.com/reaction/1509353
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Stannous Chloride | HCID 24479 | — |
| Edukt | (Benzo(1,2-b:4,5-b)dithiophene-4,8-dione) | HCID 288478 | — |
| Edukt | HCID 178443576 | HCID 178443576 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,8-Bis(2-ethylhexyl)benzo[1,2-b:4,5-b']dithiophene | HCID 59609202 | 13% |
Reaktionsschritte
To a suspension of benzo[1,2-b:4,5-b′]dithiophene-4,8-dione (25) (Beimling, P.; Koβmehl, G. Chem. Ber. 1986, 119, 3198) (4.9 g, 22.2 mmol) in 100 mL of THF was added 2-ethylhexyl magnesium bromide (111 mL, 1M in diethyl ether). The mixture was then heated at 60° C. for 24 h., and cooled to r.t. following by adding SnCl2 (13.47 g, 71.04 mmol) in 190 mL of 10% HCl. The mixture was heated at 60° C. for 24 h. THF was removed under reduced pressure. The residure was dissolved in ether, washed with water, sat. NaHCO3, brine and water. The organic layer was dried over MgSO4 and then concentrated. Column chromatography with hexane gave 1.2 g (13%) of desired product 26. 1H-NMR (400 MHz, CDCl3): ppm 7.46 (d, 2H, J=5.6 Hz), 7.42 (d, 2H, J=5.6 Hz), 3.18-3.06 (m, 4H), 1.97 (hep, 2H, J=6.4 Hz), 1.43-1.18 (m, 16H), 0.91-0.81 (m, 12H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09221944B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-72106297f42a46d294a19713264ac56a |
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| Quellennotiz | uspto-grants-2015_12 |
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