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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599029Generated: October 27, 2026

Ethylene Glycol → 2-{6-Chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol

https://huagongshe.com/reaction/1599029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
SolventAcetic AcidHCID 176—
Product2-{6-Chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanolHCID 11118967—

Reaction Steps

To a mixture of tetrahydrofuran (400 ml) and ethylene glycol (60 ml) is added with stirring sodium hydride (60% dispersion, 3.38 g) under ice-cooling, and thereto is added 4,6-dichloro-5-(4-methylphenyl)pyrimidine (20.0 g). The mixture is stirred under ice-cooling for 30 minutes, and then stirred at room temperature for two hours. The mixture is weakly acidified with acetic acid, and concentrated under reduced pressure. The residue is dissolved in ethyl acetate, and washed, dried, and concentrated to dryness under reduced pressure. The residue is crystallized from hexane to give 2-{6-chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (21.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739333
Source datasetuspto-grants-1998_04
ORD IDord-443b6a410d644885b063dcd42d3ef063
Source noteuspto-grants-1998_04