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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734341Generated: October 30, 2026

Acetamide → 4-(4-Bromophenyl)-2-methyl-1,3-oxazole

https://huagongshe.com/reaction/734341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
Reactant4-Bromophenacyl bromideHCID 7454—
Product4-(4-Bromophenyl)-2-methyl-1,3-oxazoleHCID 12873107—

Reaction Steps

4-Bromophenacyl bromide (21.3 g) and acetamide (11.3 g) were heated together at 130° C. under argon. After 2.5 h the reaction mixture was allowed to cool, and partitioned between water (150 ml) and Et2O (150 ml). The organic phase was washed with aqueous NaOH (0.5N), aqueous HCl (0.5M) and saturated aqueous NaCl solution (100 ml of each), dried (MgSO4) and evaporated to give a brown solid which was recrystallised from hexanes to give the title compound (D37) as an orange solid (4.1 g). LCMS electrospray (+ve) 239 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592347B2
Source datasetuspto-grants-2009_09
ORD IDord-55bba1c4c74d437eb615c78727c7674f
Source noteuspto-grants-2009_09