Hydrochloric Acid → 5-(1-Propynyl)pyridine-3-boronic Acid (contains varying amounts of Anhydride)

Temperature

-50 °C

3-Bromo-5-(prop-1-ynyl)pyridine (Intermediate 14, 25 g, 117 mmol), 2-methyl-tetrahydrofuran (60 mL), toluene (200 mL) and triisopropyl borate (33.2 mL, 140.78 mmol) were mixed. The mixture was cooled to −50° C. To the cold mixture was added n-BuLi (59.8 mL, 149.5 mmol) dropwise during 30 min. The mixture was stirred for 60 min. at −50° C. 2M HCl aq. (100 mL) was added. The mixture was then allowed to reach r.t. and stirred for 20 min. The organic and water phase were separated. The organic phase was extracted with NaOH (2M aq.) (2×100 mL). The water phases were combined and the pH was adjusted to pH 5. The product was extracted with 2-methyl-THF (2×100 mL). The organic phase was dried with Na2SO4, filtered and concentrated to give the title compound (16.47 g, 87% yield): 1H NMR (500 MHz, CD3OD) δ ppm 2.11 (s, 3 H) 8.21 (br. s., 1 H) 8.53 (m, 2 H); MS (APCI+) m/z 162.2 [M+H]+.

1. customto reach r.t.
2. stirringstirred for 20 min
3. customThe organic and water phase were separated
4. extractionThe organic phase was extracted with NaOH (2M aq.) (2×100 mL)
5. extractionThe product was extracted with 2-methyl-THF (2×100 mL)
6. dry with materialThe organic phase was dried with Na2SO4
7. filtrationfiltered
8. concentrationconcentrated

ORD record

ord-a43a6c5171d94c99ac1765b42338891c

Source dataset

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08415483B2