Acetone → 2-(6-Bromo-3-pyridyl)-2-propanol

Temperature

-78 °C

2,5-Dibromopyridine 3.05 g (12.5 mmol) was dissolved in 20 mL of THF and 120 mL of anhydrous ether and cooled to −78° C. 5.0 mL n-butyllithium (2.5 M, 12.5 mmol) was slowly dropped through a syringe in 30 min. After being stirred at −78° C. for 30 minutes, acetone (2 ml, 20 mmol) was added. The reaction mixture was warmed up to room temperature during two hours and then quenched by 10 ml water. The mixture was extracted twice using EtOAc. The combined extracts were dried and concentrated. After crystallization using 20% EtOAc in hexane, 1.30 g of white crystals was obtained (48% yield), MS: 215.0, 217.0 (M++1).

1. temperatureThe reaction mixture was warmed up to room temperature during two hours
2. customquenched by 10 ml water
3. extractionThe mixture was extracted twice using EtOAc
4. customThe combined extracts were dried
5. concentrationconcentrated
6. customAfter crystallization

ORD record

ord-d1512fddc44445bfab76222870a71b48

Source dataset

uspto-grants-2013_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08362003B2