Hydrochloric Acid → HCID 59245809, compound

Temperature

-78 °C

4.0 g (17.3 mmol) of dibenzoselenophene and 150 mL of dry ether were added in a 250 mL three necked flask under nitrogen. To the mixture, 11.5 mL of BuLi (1.6 M in hexane) was added slowly at room temperature. The reaction mixture was then heated to reflux for 5 hours. The reaction mixture was cooled to −78° C. and 5 mL of trimethyl borate was added. It was then left to stir at room temperature for overnight. About 50 mL of 1 M HCl was added to the reaction mixture. The organic phase was extracted with ethyl acetate and dried with sodium sulfate. The combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane was added to the solid with stirring at room temperature for 8 hours. The suspension was filtered, the solids were washed with hexane and dried, yielding 2 of white solids as the product which was confirmed by NMR

1. temperatureThe reaction mixture was then heated
2. temperatureto reflux for 5 hours
3. waitIt was then left
4. extractionThe organic phase was extracted with ethyl acetate
5. dry with materialdried with sodium sulfate
6. customThe combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane
7. additionwas added to the solid
8. stirringwith stirring at room temperature for 8 hours
9. filtrationThe suspension was filtered
10. washthe solids were washed with hexane
11. customdried
12. customyielding 2 of white solids as the product which

ORD record

ord-c08a5405d5904f36a6efde542595a009

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08945727B2