Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669805Generated: November 1, 2026

Nitroethane → 5-(4-Fluorophenyl)-3-methyl-1,2-oxazole

https://huagongshe.com/reaction/1669805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product5-(4-Fluorophenyl)-3-methyl-1,2-oxazoleHCID 12539540—

Reaction Steps

2.41 ml (22.19 mmol) of phenyl isocyanate are added dropwise at room temperature to a solution of 2 g (16.64 mmol) of 1-ethynyl-4-fluorobenzene, 0.4 ml (5.55 mmol) of nitroethane and 0.15 ml (1.11 mmol) of triethylamine in 40 ml of benzene. The reaction mixture is then stirred under reflux for 12 h. After cooling, the suspension is mixed with water (20 ml) and stirred at room temperature for a further 4 h. The precipitate is filtered off with suction and washed with benzene (10 ml). The organic phase of the filtrate is separated off, dried with magnesium sulfate and concentrated. The residue is purified by column chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 9:1). 0.62 g (63% of theory) of the title compound is obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989633B2
Source datasetuspto-grants-2011_08
ORD IDord-49495c128ba34c28aa01ed01b4c80247
Source noteuspto-grants-2011_08