HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925212Generated: October 29, 2026
Acetic Anhydride → 1-[6-(4-Fluorophenyl)imidazo[2,1-b][1,3]oxazol-5-yl]ethanone
https://huagongshe.com/reaction/1925212
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-(4-Fluorophenyl)-imidazo[2,1-b]oxazole | HCID 57433610 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-[6-(4-Fluorophenyl)imidazo[2,1-b][1,3]oxazol-5-yl]ethanone | HCID 16726482 | 86% |
Reaction Steps
To a mixture of 6-(4-fluorophenyl)-imidazo[2,1-b]oxazole (2675 g, 13.23 mol) and acetic anhydride (6.35 l) is added 160 ml of concentrated sulfuric acid. The reaction mixture is heated at 135° C. for 1.5 hours, then cooled to 80° C. with an ice bath. The reaction mixture is slowly quenched with 12.5 l of water. The solids are stirred overnight, filtered and air-dried. The solids are again suspended in water (15 l), stirred overnight, filtered, and washed with water (4 l) and then with toluene (4 l). The solid is dried under vacuum at 60° C., to give 2771 g (86%) of a dark brown 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 |
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| Patent number | US08178672B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4318b618e5674f148c29af60b037923d |
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| Source note | uspto-grants-2012_05 |
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