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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544311Generated: October 31, 2026

Dimethyl Sulfoxide → 5-(2-Fluoro-6-methoxyphenyl)-1,3-oxazolidine-2,4-dione

https://huagongshe.com/reaction/544311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantHCID 13092030HCID 13092030—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethanolHCID 887—
Product5-(2-Fluoro-6-methoxyphenyl)-1,3-oxazolidine-2,4-dioneHCID 13092033—

Reaction Conditions

Temperature155 °C

Reaction Steps

5-(2,6-Difluorophenyl)oxazolidine-2,4-dione (2.0 g., 9.4 mmoles) was dissolved in 50 ml. of dimethylsulfoxide. Methanol (5 ml.) and then potassium tertbutoxide (2.11 g., 18.8 mmoles) were then added and the reaction mixture heated in an oil bath maintained at 155° C. for 4 hours. The reaction mixture was cooled to room temperature, poured into 200 ml. of 1N hydrochloric acid and extracted with three portions of ethyl acetate. The combined organic extracts were washed with water and then brine, dried over anhydrous magnesium sulfate, filtered and concentrated to solids. The solids were taken up in 1N sodium hydroxide, and the solution washed with three portions of ethyl acetate and then acidified with 1N hydrochloric acid to precipitate purified 5-(2-fluoro-6-methoxyphenyl)oxazolidine-2,4-dione (1.32 g., 62 %; m.p. 138°-142° C.). For analysis, the product was recrystallized from toluene (930 mg. recovered; m.p. 139°-141° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448971
Source datasetuspto-grants-1984_05
ORD IDord-f4d75fd432054a4a9b3262fb1bb59415
Source noteuspto-grants-1984_05