Hydrochloric Acid → HCID 22316969, compound

To a solution of 3-bromothiophene (8.15 g, 50 mmol) in THF (20 ml) at -78° C. under an argon atmosphere was added n-butyllithium (2.5M solution in hexane, 20 ml, 50 mmol) dropwise and the resultant solution was stirred at -78° C. for 45 min. This solution was added to a solution of triisopropyl borate (9.4 g, 50 mmol) in THF at -78° C. over 30 min through a steel cannula. The resultant reaction mixture was stirred at room temperature for 12 h and was decomposed by the addition of 100 ml 1N HCl. The aqueous layer was extracted with ether (2×100 ml) and the combined organic layer was extracted with 1M NaOH (3×30 ml), the aqueous extract was acidified with concentrated HCl to pH 2 and extracted with ether (3×50 ml). The combined ether extract was washed once with water, dried over MgSO4 and filtered. Removal of the solvent gave 3-thenylboronic acid as a solid (5.2 g, 80% yield).

1. customThe resultant reaction mixture
2. extractionThe aqueous layer was extracted with ether (2×100 ml)
3. extractionthe combined organic layer was extracted with 1M NaOH (3×30 ml)
4. extractionthe aqueous extract
5. extractionextracted with ether (3×50 ml)
6. extractionThe combined ether extract
7. washwas washed once with water
8. dry with materialdried over MgSO4
9. filtrationfiltered
10. customRemoval of the solvent

ORD record

ord-14482fc086ad42509970a05b9b203bb9

Source dataset

uspto-grants-1996_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05571821