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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908808Generated: October 28, 2026

Methanol → (4-BROMO-6-METHYL-PYRIDIN-2-YL)-METHANOL

https://huagongshe.com/reaction/1908808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium PersulfateHCID 62648—
Reactant4-Bromo-2-methylpyridineHCID 2762835—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product(4-BROMO-6-METHYL-PYRIDIN-2-YL)-METHANOLHCID 67027007—

Reaction Steps

To a solution of 4-bromo-2-methyl-pyridine (5.70 g, 32.14 mmol) in methanol (100 mL), H2SO4 (0.3 mL) is added. The mixture is heated to reflux before a solution of ammonium peroxydisulfate (7.33 g, 32.14 mmol) in water (53 mL) is carefully added. The mixture is stirred at reflux für 2 h before two more portions of ammonium peroxydisulfate (2×7.33 g) is added as a sat. aq. solution. Stirring is continued at reflux for 3 h. Methanol is removed under reduced pressure and the remaining solution is diluted with sat. aq. NaHCO3 solution and extracted with EA. The org. extract is dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 3:7 to give (4-bromo-6-methyl-pyridin-2-yl)-methanol (1.31 g) as pale yellow solid; LC-MS: tR=0.31 min; [M+1]+=201.96; 1H NMR (CDCl3): δ 2.55 (s, 3H), 3.59 (s br, 1H), 4.72 (s br, 2H), 7.28 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598208B2
Source datasetuspto-grants-2013_12
ORD IDord-7e025bac529c49719d72726152d01bac
Source noteuspto-grants-2013_12