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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923495Generated: November 4, 2026

Acetic Anhydride → HCID 118308722, compound

https://huagongshe.com/reaction/923495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131734993HCID 131734993—
SolventDichloromethaneHCID 6344—
ProductHCID 118308722HCID 118308722—

Reaction Steps

To a solution of 146 mg of tert-butyl 4-(N′-hydroxycarbamimidoyl)-2,2,4-trimethyl-1,3-oxazolidine-3-carboxylate in 4 ml of dichloromethane was added 55 μl of acetic anhydride, followed by stirring at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and to the obtained residue were added 4 ml of DMF, followed by stirring at 110° C. for 15 hours. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 113 mg of tert-butyl 2,2,4-trimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-oxazolidine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-923dfcf376d94d5e9f015b0ede2dc92a
Source noteuspto-grants-2016_03