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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220063Generated: October 30, 2026

6-Methyl-2-pyridinecarboxaldehyde → 1-(6-Methylpyridin-2-yl)ethanol

https://huagongshe.com/reaction/2220063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methyl-2-pyridinecarboxaldehydeHCID 70737—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Methylpyridin-2-yl)ethanolHCID 353138100%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a −60° C. solution of 6-methyl-pyridine-2-carbaldehyde (25 g, 206 mmol) in tetrahydrofuran (200 mL) was added methyl magnesium bromide (200 mL, 1.4 M in tetrahydrofuran/toluene, 1.36 equiv) over 40 minutes. The reaction mixture was slowly warmed to −10° C. over 90 minutes, and then slowly quenched with saturated aqueous ammonium chloride (75 mL). The liquid phase was decanted from the solids and concentrated in vacuo. The resulting residue was dissolved in methylene chloride, dried over magnesium sulfate, and concentrated in vacuo to yield the title compound (28 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417041B2
Source datasetuspto-grants-2008_08
ORD IDord-c514cf88f4374c6b9016ab91071e4204
Source noteuspto-grants-2008_08