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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163950Generated: October 29, 2026

Acetic Anhydride → HCID 13093538, compound

https://huagongshe.com/reaction/1163950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-(2-Chloro-6-methoxyphenyl)-1,3-oxazolidine-2,4-dioneHCID 13092015—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13093538HCID 13093538—

Reaction Steps

5-(2-Chloro-6-methoxyphenyl)oxazolidin-2,4-dione (1.21 g., 5 mmoles) was dissolved in 10 ml. of tetrahydrofuran. Acetic anhydride (613 mg. 0.57 ml. 6 mmoles) was added and the solution stirred at room temperature for 44 hours. The reaction mixture was concentrated to an oil, partitioned between chloroform and saturated sodium bicarbonate. The chloroform layer was washed with fresh bicarbonate and then brine, dried over anhydrous magnesium sulfate, filtered, and concentrated to solid. Repulp of the residue in about 50 ml. of ether gave 3-acetyl-5-(2-chloro-6-methoxyphenyl)oxazolidin-2,4-dione (790 mg., 56%; m.p. 132°-135° C. m/e 285/283).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367234
Source datasetuspto-grants-1983_01
ORD IDord-cf61406a8411463ab5ecd2fdfe6627c8
Source noteuspto-grants-1983_01