Trimethyltin chloride → 2,5‐ bis(triMethylstannyl)th ieno[3,2‐b]thiophene

Temperature

-78 °C

In a 3-neck round bottom flask equipped with an argon inlet and an addition flannel, thieno[3,2-b]thiophene (7.5 g, 54 mmol) was dissolved in tetrahydrofuran (1 L). After the solution was cooled to −78° C. using an isopropanol/dry ice bath, t-BuLi (100 mL, 170 mmol) was transferred by cannula to the addition funnel. The organolithium reagent was then added dropwise. After completion of the addition, the mixture was stirred for 20 min at −78° C. then warmed up with an isopropanol bath at room temperature for 30 minutes during which a yellow precipitate formed. The solution was cooled back at −78° C., and after cannula transfer to the addition funnel, trimethyltin chloride (200 mL of 1 M solution in THF, 200 mmol) was added dropwise. During addition of trimethyltin chloride, the precipitate disappeared and the solution turned light brown. After warming to room temperature the solution was stirred for 30 minutes then was poured into ice-cold water. The aqueous phase was further extracted with hexane. The combined organic phase were washed with cold water then dried with magnesium sulfate. After filtration, the solvent is evaporated under vacuum to yield a grey-brown solid. The product was purified by precipitation of a chloroform solution into methanol followed by filtration (13.2 g, 53%).

1. customIn a 3-neck round bottom flask equipped with an argon inlet
2. additionAfter completion of the addition
3. temperaturethen warmed up with an isopropanol bath at room temperature for 30 minutes during which a yellow precipitate
4. customformed
5. temperatureThe solution was cooled back at −78° C.
6. temperatureAfter warming to room temperature the solution
7. stirringwas stirred for 30 minutes
8. additionthen was poured into ice-cold water
9. extractionThe aqueous phase was further extracted with hexane
10. washThe combined organic phase were washed with cold water
11. dry with materialthen dried with magnesium sulfate
12. filtrationAfter filtration
13. customthe solvent is evaporated under vacuum
14. customto yield a grey-brown solid
15. customThe product was purified by precipitation of a chloroform solution into methanol
16. filtrationfollowed by filtration (13.2 g, 53%)

ORD record

ord-67597bbd55fc4e30ad7f2b45e3f0337a

Source dataset

uspto-grants-2015_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08968885B2