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!

(2-METHYL-PYRIDIN-3-YL)-METHANOL synthesis

4synthesis methods
-

Yield:76915-53-2 3.52 g

Reaction Conditions:

with phosphorus tribromide in dichloromethane at 0 - 20; for 1.5 h;

Steps:

b Step b:

To a 0 °C mixture of(2-methylpyridin-3-yl) methanol (1.41 g, 11.45 mmol) in DCM (20 mL) was added PBr3 (1.86 g, 6.87 mmol) dropwise. The resulting mixture was allowed to warm to RT and stirred for 1.5 h. The reaction mixture was taken to pH 8 using aq. NaOH (5 M, 10 mL). The aqueous layer was separated and the organic layer was washed with brine (1 x 20 mL), dried over anhydrous Na2504 and concentrated under reduced pressure to give 3-(bromomethyl)-2-methylpyridine as a yellow oil (3.52 g) which was used in next step without any further purification. MS: m/z 186 (M+H) .

References:

WO2018/172984,2018,A1 Location in patent:Page/Page column 66