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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStannous ChlorideHCID 24479—
Edukt(Benzo(1,2-b:4,5-b)dithiophene-4,8-dione)HCID 288478—
EduktHCID 178443576HCID 178443576—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,8-Bis(2-ethylhexyl)benzo[1,2-b:4,5-b']dithiopheneHCID 5960920213%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09221944B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-72106297f42a46d294a19713264ac56a
Quellennotizuspto-grants-2015_12