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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241864Generated: October 25, 2026

2-Methylpyrimidine-5-carbaldehyde → 1-(2-Methylpyrimidin-5-yl)ethanol

https://huagongshe.com/reaction/241864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylpyrimidine-5-carbaldehydeHCID 3160970—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Methylpyrimidin-5-yl)ethanolHCID 54772447—

Reaction Steps

To a stirred solution of 2-methylpyrimidine-5-carbaldehyde (5.00 g, 38.9 mmol) in tetrahydrofuran (85 mL) was slowly added 33 mL of 1.4 M methylmagnesium bromide solution in tetrahydrofuran at 0° C. The mixture was stirred at room temperature for 1 hour and then quenched with water (50 mL) and extracted with EtOAc (3×200 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography (0-100% EtOAc/hexane) to afford a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653091B2
Source datasetuspto-grants-2014_02
ORD IDord-838c6debebd24135ba7330f32fb2be37
Source noteuspto-grants-2014_02