Diethyl Ether → 2-(5-Bromo-3-pyridyl)propan-2-ol

To a cooled (−78° C.) solution of 3-acetyl-5-bromo pyridine (1.98 g, 9.90 mmol) in tetrahydrofuran (33 mL) was added dropwise a solution of methyl magnesium bromide in diethyl ether (3.0 M, 6.60 mL, 19.8 mmol). The reaction was warmed to room temperature, and the resulting mixture was stirred at room temperature overnight. The reaction was then quenched with saturated aqueous ammonium chloride solution and extracted with diethyl ether. The organic extracts were combined, washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by flash chromatography on silica gel (0-60% ethyl acetate in hexanes) provided the title compound: LCMS m/z 217.83 [M+11]+; 1H NMR (500 MHz, CDCl3) δ 8.61 (s, 1H), 8.53 (s, 1H), 8.01 (d, J=1.9 Hz, 1H), 2.38 (br s, 1H), 1.61 (6H).

1. customThe reaction was then quenched with saturated aqueous ammonium chloride solution
2. extractionextracted with diethyl ether
3. washwashed with brine
4. dry with materialdried over magnesium sulfate
5. filtrationfiltered
6. concentrationconcentrated
7. customPurification by flash chromatography on silica gel (0-60% ethyl acetate in hexanes)

ORDレコード

ord-83eeb3bbb294465dae11bfec4f09120d

出典データセット

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09173873B2