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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828777Generated: November 4, 2026

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

https://huagongshe.com/reaction/1828777

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 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 1C (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 numberUS07060720B2
Source datasetuspto-grants-2006_06
ORD IDord-dcdfc590cddc4176983c2996a52f6756
Source noteuspto-grants-2006_06