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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783808Generated: October 31, 2026

Acetic Anhydride → 1-[6-(4-Fluorophenyl)imidazo[2,1-b][1,3]oxazol-5-yl]ethanone

https://huagongshe.com/reaction/1783808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant6-(4-Fluorophenyl)-imidazo[2,1-b]oxazoleHCID 57433610—
CatalystSulfuric AcidHCID 1118—
Product1-[6-(4-Fluorophenyl)imidazo[2,1-b][1,3]oxazol-5-yl]ethanoneHCID 1672648272.6%

Reaction Steps

A solution of 6-(4-fluorophenyl)-imidazo[2,1-b]oxazole (2.5 g, 0.0124 mol) in acetic anhydride (60 ml) was heated to 140° C. and then treated with concentrated sulfuric acid (5 drops). After 15 minute at that temperature, HPLC showed clean conversion and the reaction mixture was quenched by the addition of ice cold water (150 ml). The mixture was extracted with ethyl acetate (3×150 ml). The combined extracts were washed with a saturated aqueous sodium chloride solution (300 ml), dried over magnesium sulfate and concentrated in vacuo as a brown solid. Trituration from a mixture of hexanes/ethyl acetate (1:1) provided 2.2 g (72.6%) of a pale yellow solid. M.p.=173° C.; 300 MHz 1H NMR (DMSO-d6) δ 8.25-8.19 (m, 2H), 7.75-7.68 (m, 2H), 7.35-7.25 (m, 2H), 2.15 (s, 3H). LCMS: 245 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501430B2
Source datasetuspto-grants-2009_03
ORD IDord-6b818454fd0940c896fa7fd5a9a53ce8
Source noteuspto-grants-2009_03