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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647801Generated: October 30, 2026

Ethanol → 5-Ethoxypyrimidine

https://huagongshe.com/reaction/1647801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-BromopyrimidineHCID 78344—
ReactantSodiumHCID 5360545—
Product5-EthoxypyrimidineHCID 1992168825.6%

Reaction Steps

Sodium (2.89 g. 125.8 mmol) was dissolved in ethanol (110 mL) and 5-bromopyrimidine (10.0 g, 62.9 mmol) added. The reaction was heated at 120° in an autoclave for 17 h and then allowed to stand at 23° for 60 h. The ethanol was removed under reduced pressure and water (5 mL) added to the concentrate. The aqueous phase was extracted with CH2Cl2 (4×100 mL). The combined organic extracts were washed with saturated NaCl solution, dried with anhydrous K2CO3, filtered, and concentrated under reduced pressure. Silica gel chromatography (Hexane/EtOAc; 70:30) of the concentrate yielded 5-ethoxypyrimidine (2.00 g, 25.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434154
Source datasetuspto-grants-1995_07
ORD IDord-77972697092b4fd59903f046ff5a45d4
Source noteuspto-grants-1995_07