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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596796Generated: October 31, 2026

Acetic Acid → 5-Methyl-4-[2-(7-nitro-benzothiophene-4-yloxy)-ethyl]-2-phenyl-oxazole

https://huagongshe.com/reaction/1596796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitric AcidHCID 944—
ReactantSodium CarbonateHCID 10340—
Reactant4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzothiopheneHCID 11232947—
SolventWaterHCID 962—
Product5-Methyl-4-[2-(7-nitro-benzothiophene-4-yloxy)-ethyl]-2-phenyl-oxazoleHCID 15485664—

Reaction Conditions

Temperature60 °C

Reaction Steps

286 g (0.853 mol) of 4-[2-(benzothiophene-4-yloxy)-ethyl]-5-methyl-2-phenyl-oxazole were suspended in 6.31 of glacial acetic acid. Temperature was raised to 60° C. The resulting clear solution was cooled to 25° C. 132 ml (3.18 mol) of 100% nitric acid were added within 3 minutes. The reaction miture was cooled below 30° C. After crystallization the suspension was stirred at 18 to 20° C. for 1 hour. The precipitate was filtered with suction and washed with 2×600 ml of tert-butyl methyl ether. The residue was suspended in 4 l of acetic ester for 15 minutes. 200 g (1.9 mol) of sodium carbonate in 3 l water were added. The resulting suspension was stirred for 1 hour. Acetic ester was distilled off followed by addition of 2 l of water. The suspension was stirred for 30 minutes. The precipitate was filtered with suction, washed with water and dried (50° C., 24 hours).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291685B1
Source datasetuspto-grants-2001_09
ORD IDord-c0343d93ffa64139bda5dcdcd4b3788b
Source noteuspto-grants-2001_09