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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167071Generated: October 29, 2026

Methanol → 5-(2-Methoxy-4-nitrophenyl)oxazole

https://huagongshe.com/reaction/1167071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant2-Methoxy-4-nitrobenzaldehydeHCID 2759599—
SolventWaterHCID 962—
Product5-(2-Methoxy-4-nitrophenyl)oxazoleHCID 1019834084%

Reaction Conditions

Temperature64 °C

Reaction Steps

To a 5 L three necked round bottom flask equipped with a condenser and a mechanical stirrer was placed 1B (146.3 g, 0.8076 mol), TOSMIC (157.7 g, 0.8077 mol), K2CO3 (116.6 g, 0.8075 mol) and MeOH (2.5 L). The mixture was heated to reflux under N2 and stirred for 3 hours. Water (1.25 L) was added drop-wise while maintaining the pot temperature between 59-69° C. The resulting slurry was cooled to room temperature, and then to 5° C. with an ice-water bath. After stirring for 30 minutes at 5° C., the slurry was filtered. The resulting cake was washed with water (3×400 mL) and dried in a vacuum oven at 45° C. for 20 hours to give 5-(4-nitro-2-methoxyphenyl)oxazole (IC, 148.5 g, 84%) as a yellow-reddish solid. 1H NMR (CDCl3) d 8.02 (s, 1H), 7.97 (d, J=2 Hz, 1H), 7.95 (d, J=2 Hz, 1H), 7.86 (s, 1H), 7.78 (s, 1H), 4.11 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617323B2
Source datasetuspto-grants-2003_09
ORD IDord-df7c539461fc483ca1291e7137f5badd
Source noteuspto-grants-2003_09