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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-(4-Fluorophenyl)-imidazo[2,1-b]oxazole | HCID 57433610 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | 1-[6-(4-Fluorophenyl)imidazo[2,1-b][1,3]oxazol-5-yl]ethanone | HCID 16726482 | 72.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07501430B2 |
|---|
| Source dataset | uspto-grants-2009_03 |
|---|
| ORD ID | ord-6b818454fd0940c896fa7fd5a9a53ce8 |
|---|
| Source note | uspto-grants-2009_03 |
|---|