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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784662Generated: November 3, 2026

Methyl iodide → 4-(1,2,5,6-Tetrahydro-1-methyl-3-pyridinyl)benzenemethanol

https://huagongshe.com/reaction/1784662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-(Pyridin-3-yl)benzaldehydeHCID 3693046—
ReactantSodium borohydrideHCID 4311764—
SolventDichloromethaneHCID 6344—
Product4-(1,2,5,6-Tetrahydro-1-methyl-3-pyridinyl)benzenemethanolHCID 6711738372.1%

Reaction Steps

Methyl iodide (0.8 ml, 12.9 mmol) was added to a solution of 4-(3-pyridyl)benzaldehyde (0.78 g, 4.3 mmol) in dichloromethane and stirred 2 days. Additional methyl iodide (0.8 ml, 12.9 mmol) was added and stirred for 3 hr. After removal of the solvent, methanol was added to the residue and ice-cooled. Sodium tetrahydroborate (6.4 g, 17.0 mmol) was added to the solution and stirred for 1.5 hr with warming to room temperature. Organic solvents were removed under reduced pressure after addition of water and extracted with ethyl acetate, washed with water and brine and dried over sodium sulfate. After removal of the solvent under reduced pressure, residue was purified by silica gel chromatography (eluent ethyl acetate to methanol) to give 3-(4-hydroxymethylphenyl)-1-methyl-1,2,5,6-tetrahydropyridine (0.63 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504411B2
Source datasetuspto-grants-2009_03
ORD IDord-4a443f0ff195436fbdf1639a06c2e660
Source noteuspto-grants-2009_03