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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512688Generated: October 30, 2026

4-Bromo-3,5-dimethoxybenzaldehyde → 5-(4-Bromo-3,5-dimethoxyphenyl)oxazole

https://huagongshe.com/reaction/512688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3,5-dimethoxybenzaldehydeHCID 3015579—
ReactantToluenesulfonylmethyl isocyanideHCID 53627694—
SolventMethanolHCID 887—
Product5-(4-Bromo-3,5-dimethoxyphenyl)oxazoleHCID 5843215039%

Reaction Steps

A solution of 4-bromo-3,5-dimethoxybenzaldehyde (5.04 g, 20.57 mmole) and toluenesulfonylmethyl isocyanide (4.22 g, 21.6 mmole) in MeOH (50 ml) was heated at reflux for 3 hrs. After evaporation to near dryness, H2O (50 ml) and EtOAc (200 ml) were added with stirring. The organic layer was separated and washed with brine (50 ml), dried over Na2SO4 and concentrated in vacuo. Et2O (50 ml) was added with swirling and the product was collected by filtration, washed with Et2O (2×25 ml) and dried giving 5-(4-bromo-3,5-dimethoxyphenyl)oxazole as a pale yellow solid (2.25 g, 39% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102643B2
Source datasetuspto-grants-2015_08
ORD IDord-d530a173e83047f19c37e048a5ee7b82
Source noteuspto-grants-2015_08