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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33563Generated: October 29, 2026

Methanol → 2-Acetylamino-4-(naphth-1-yl)oxazole

https://huagongshe.com/reaction/33563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4-(naphth-1-yl)oxazoleHCID 10307957—
SolventDichloromethaneHCID 6344—
Product2-Acetylamino-4-(naphth-1-yl)oxazoleHCID 59796840—

Reaction Steps

To a cooled (ice/salt bath) mixture of 2-amino-4-(naphth-1-yl)oxazole (1)(0.5 g) and triethylamine (0.8 ml) in anhydrous dichloromethane (5 ml) was added dropwise acetyl chloride (0.2 ml) over a minute. The resulting mixture was warmed to room temperature and left overnight. Further acetyl chloride (0.1 ml) was added and the mixture left for a further hour. Dichloromethane (40 ml) and few drops of methanol were added. The mixture was washed twice with brine, dried with sodium sulphate, filtered and evaporated in vacuo. The title compound (9) (0.35 g; m.p. 188-190° C.) was obtained following silica gel column chromatography of the residue in 2% methanol in chloroform.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429607B2
Source datasetuspto-grants-2008_09
ORD IDord-4a542a07cdbf48b783167e4decab0fd8
Source noteuspto-grants-2008_09