Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

Pyridine, 3-bromo-4-(3-bromopropyl)- synthesis

3synthesis methods
3-BROMO-4-(3-HYDROXYPROPYL)PYRIDINE

229184-01-4
7 suppliers
inquiry

Pyridine, 3-bromo-4-(3-bromopropyl)-

216012-95-2
1 suppliers
inquiry

-

Yield:216012-95-2 72%

Reaction Conditions:

with carbon tetrabromide;triphenylphosphine in dichloromethane at 0 - 20; for 0.5 h;

Steps:

192.4 Step 4: Synthesis of 3-bromo-4-(3-bromopropyl)pyridine

To a solution of 3-(3-bromo-4-pyridyl)propan-1-ol (1.95 g, 9.0 mmol) in dichloromethane (50 mL) was added triphenylphosphine (3.55 g, 13.5 mmol) at room temperature, followed by addition of carbon tetrabromide (4.49 g, 13.5 mmol) at 0 °C. After stirring at room temperature for 0.5 hour, the reaction mixture was concentrated under reduced pressure. Purification via silica gel column chromatography (ethyl acetate/petroleum ether) afforded the title compound as a light-yellow oil. Yield: 2.10 g, 72%. LCMS (ESI) m/z: 280.0 (M+H).1H NMR (DMSO-d6, 300 MHz): δ 8.67 (s, 1H), 8.46 (d, 1H, J=5.1 Hz), 7.40 (d, 1H, J=5.1 Hz), 3.58 (t, 2H, J=6.6 Hz), 2.72-2.91 (m, 2H), 2.03-2.17 (m, 2H).

References:

WO2022/109492,2022,A1 Location in patent:Page/Page column 552-554