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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938108Generated: October 27, 2026

Ethanol → 2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine

https://huagongshe.com/reaction/1938108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantChloroformHCID 6212—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Acetylphenyl)-5-decyloxypyrimidineHCID 19694901—
SolventWaterHCID 962—
Product2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidineHCID 2146828099.9%

Reaction Steps

To a mixed solvent of 200 ml of ethanol and 100 ml of chloroform were added 35.5 g (0.1 mole) of 2-(4-acetylphenyl)-5-decyloxypyrimidine, and while maintaining the temperature at 30° to 35° C., 2.65 g (0.07 mole) of sodium borohydride were gradually added thereto. After stirring at the same temperature for 4 hours, the reaction mixture was poured into 500 ml of water and extracted with 400 ml of ethyl acetate. The organic phase was washed sufficiently, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 35.6 g (yield: 99.9 %) of 2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693251
Source datasetuspto-grants-1997_12
ORD IDord-c9046b081e0f4cf0b15ce782fba6c387
Source noteuspto-grants-1997_12