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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/1160

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 21468280100.3%

Reaction Steps

35.5 g (0.1 mo1) of 2-(4-acetylphenyl)-5-decyloxypyrimidine, 300 ml of ethanol and 300 ml of chloroform were supplied into a four-necked flask equipped with a stirrer and a thermometer. Then 2.8 g (0.075 mol) of sodium borohydride was added at 30°-40° C. and the mixture was stirred at the same temperature for 4 hours. The resulting reaction mixture was poured into 500 ml of water, followed by extraction and liquid separation, and the obtained chloroform layer was washed with water, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 35.8 g of 2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine (II-c-11) (yield: 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723610
Source datasetuspto-grants-1998_03
ORD IDord-8266c5cd4a68414b8c3137da7bc01eef
Source noteuspto-grants-1998_03