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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428572Generated: October 25, 2026

Hydrochloric Acid → 2-(4-Iodophenyl)oxazole

https://huagongshe.com/reaction/428572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl MethanesulfonateHCID 4156—
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantN-(2,2-dimethoxyethyl)-4-iodobenzamideHCID 10903782—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Iodophenyl)oxazoleHCID 9860258—

Reaction Conditions

Temperature140 °C

Reaction Steps

Under an inert atmosphere, methanesulfonic acid (141 g, 1.46 mol) was added to a mixture of amide acetal (25 g, 74.6 mmol) and phosphorus pentoxide (25 g, 176 mmol). The reaction mixture was heated at 140° C. for about 12 hours. The reaction mixture was cooled to 0° C. and 150 mL of water was added while maintaining the reaction temperature below 40° C. The pH of the reaction mixture was adjusted to 12.5-13 with 50% sodium hydroxide and the reaction mixture was heated at ca. 45° C. to hydrolyze the carcinogenic byproduct methyl methanesulfonate. The reaction mixture was cooled to ambient temperature and 100 mL of tetrahydrofuran was added. The pH was adjusted to 5 with concentrated hydrochloric acid and the layers were separated. The spent aqueous phase was extracted twice with 100 mL of acetone. The rich organic extracts were combined and 200 mL of water was added to effect crystallization. The crystal slurry was filtered, washed and dried in vacuo at <50° C., to give 17 g (84 M %, HPLC area % >99) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313308B1
Source datasetuspto-grants-2001_11
ORD IDord-09ef5616e89c404e839fb6d929e1f4bf
Source noteuspto-grants-2001_11