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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434845Generated: October 29, 2026

Acetic Anhydride → HCID 13093538, compound

https://huagongshe.com/reaction/434845

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 numberUS04399296
Source datasetuspto-grants-1983_08
ORD IDord-c21c3b18f70046ad92e4d30b7aaec0fd
Source noteuspto-grants-1983_08