Iodine → 1-(5-Bromopyridin-3-yl)cyclopentanol

Temperature

65 °C

A few drops of 1,4-dibromobutane and 25 ml of tetrahydrofuran are added to a round-bottomed flask containing 2.25 g of magnesium chips (92.6 mmol) and an iodine crystal. The mixture is heated at 65° C. until decolorization is obtained and then a solution of 1,4-dibromobutane (10 g, 46.3 mmol) in 50 ml of tetrahydrofuran is added dropwise. The reaction mixture is heated at 65° C. for 4 hours and then cooled to 0° C. A solution of ethyl 2-bromonicotinate (10 g, 46.3 mmol) in 60 ml of tetrahydrofuran is then added. The reaction mixture is cooled to room temperature and stirred for 16 hours. The reaction mixture is slowly poured at 0° C. into a saturated aqueous ammonium chloride solution and then the medium is extracted with ethyl acetate. The organic phase is washed with water and then with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 70/30). The title product (3.6 g) is obtained in the form of a white solid.

1. customis obtained
2. temperatureThe reaction mixture is heated at 65° C. for 4 hours
3. temperaturecooled to 0° C
4. temperatureThe reaction mixture is cooled to room temperature
5. extractionthe medium is extracted with ethyl acetate
6. washThe organic phase is washed with water
7. dry with materialwith a saturated aqueous sodium chloride solution, dried over sodium sulfate
8. filtrationfiltered
9. concentrationconcentrated under reduced pressure
10. customThe residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 70/30)

ORD record

ord-31ae59e01e5c4fbb8e0a9518bb8379cd

Source dataset

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07163957B2