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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497217Generated: October 30, 2026

4-Bromophenacyl bromide → 4-(4-Bromophenyl)-1,3-oxazole

https://huagongshe.com/reaction/497217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium formateHCID 2723923—
SolventFormic AcidHCID 284—
Product4-(4-Bromophenyl)-1,3-oxazoleHCID 2231659526%

Reaction Steps

To a stirred solution, of 2,4′-dibromoacetophenone (9.66 g, 34.8 mmol) in formic acid (42 ml) was added ammonium formate (7.58 g. 120.6 mmol), and the mixture was heated at reflux temperature for 3 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 50% NaOH aqueous solution. The whole was extracted with CH2H2. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:5) to give title compound (2.0 g, 26% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-eae98bd690464090b6b4da023849f2a7
Source noteuspto-grants-2005_09