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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862270Generated: November 1, 2026

Methyl Lactate → 5-Benzyloxy-4-{1-(methoxycarbonyl)ethoxy}pyrimidine

https://huagongshe.com/reaction/1862270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl LactateHCID 11040—
ReactantSodium hydrideHCID 24758—
Reactant5-(Benzyloxy)-4-chloropyrimidineHCID 13607724—
SolventTetrahydrofuranHCID 8028—
Product5-Benzyloxy-4-{1-(methoxycarbonyl)ethoxy}pyrimidineHCID 18619229—

Reaction Steps

Sodium hydride is added to a mixture of 5-benzyloxy-4-chloropyrimidine, methyl lactate and tetrahydrofuran at 0° C. The mixture is stirred at room temperature for 1 hour, then, stirred for 30 minutes at 90° C. The reaction solution is cooled to room temperature, then, poured into ice water, and extracted with ethyl acetate. The organic layer is washed with dilute hydrochloric acid and saturated saline, dried over anhydrous magnesium sulfate, and concentrated. The residue is subjected to silica gel column chromatography to obtain 5-benzyloxy-4-{1-(methoxycarbonyl)ethoxy}pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06537948B1
Source datasetuspto-grants-2003_03
ORD IDord-44c2343bffa247c1bd8b29b9190ebe5b
Source noteuspto-grants-2003_03