3-Ethynylpyridine → 3-((E)-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)ethenyl)pyridine

HRID 2383652Notes

Reaction equation

[C:1]([C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1)#[CH:2].[CH3:9][C:10]1([CH3:17])[C:14]([CH3:16])([CH3:15])[O:13][BH:12][O:11]1>C1(C)C=CC=CC=1>[CH3:9][C:10]1([CH3:17])[C:14]([CH3:16])([CH3:15])[O:13][B:12](/[CH:2]=[CH:1]/[C:3]2[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=2)[O:11]1

Participants

Conditions

Temperature: 50 °C

Procedure

An oven-dried round-bottom flask was cooled under N2 (g) and then charged with 3-ethynyl pyridine (104 mg, 1 mmol), toluene (4 mL), and 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.73 mL, 5 mmol). The mixture was purged with argon for 15 min HRuCl(CO)(PPh3)3 (73 mg, 0.05 mmol) was then added and the reaction heated to 50° C. for 18 h. The reaction was quenched with NaHCO3 (sat.) (10 mL), extracted with EtOAc, and the organic layer washed with brine (10 mL) and then dried over MgSO4. The solvent was removed and the resulting residue purified by column chromatography (silica gel, Hexanes/EtOAc, 1:1) to give the title compound as a white solid (115 mg, 50%). 1H NMR (400 MHz, CDCl3) δ 8.69 (s, 1H) 8.52 (d, 1H, J=4.8 Hz), 7.81 (d, 1H, J=7.8 Hz), 7.38 (d, J=18.6 Hz, 1H), 7.28-7.26 (m, 1H), 6.26 (d, 1H, J=18.5 Hz), 1.33 (s, 12H).

Workup

temperatureAn oven-dried round-bottom flask was cooled under N2 (g)
additionwas then added
customThe reaction was quenched with NaHCO3 (sat.) (10 mL)
extractionextracted with EtOAc
washthe organic layer washed with brine (10 mL)
dry with materialdried over MgSO4
customThe solvent was removed
customthe resulting residue purified by column chromatography (silica gel, Hexanes/EtOAc, 1:1)

Sources & evidence

ORD record: ord-b1b2844a4706400fa4cac2324d549877
Source dataset: uspto-grants-2012_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08263596B2

Reaction notes

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