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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884905Generated: November 1, 2026

Benzyl Alcohol → HCID 58148151, compound

https://huagongshe.com/reaction/884905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 58148249HCID 58148249—
SolventWaterHCID 962—
ProductHCID 58148151HCID 58148151—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2.07 g of 5-tert-butyl-2-(3-fluoropyridin-4-yl)benzoxazole, 4.23 g of potassium carbonate and 8 ml of benzyl alcohol was stirred while heating at 100° C. for 8.5 hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2.2 g of 2-(3-benzyloxypyridin-4-yl)-5-tert-butylbenzoxazole (hereinafter, referred to as “active compound 102”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242133B2
Source datasetuspto-grants-2012_08
ORD IDord-bdb5b994c88c4a6381578c46f3a259cc
Source noteuspto-grants-2012_08