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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016772Generated: October 30, 2026

Acetic Anhydride → HCID 22039040, compound

https://huagongshe.com/reaction/1016772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178506516HCID 178506516—
SolventDimethylformamideHCID 6228—
ProductHCID 22039040HCID 22039040—

Reaction Steps

A mixture of 1.34 g of (E)- and/or (Z)-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-N-hydroxy-4,5-dimethoxy-benzamidine, 1.20 ml of DBU and 0.61 ml of acetic anhydride in 50 ml of DMF was stirred for 1 hr. at room temperature and subsequently for 2 hrs. at 80° C. Subsequently, the DMF was removed in a vacuum and the residue was taken up in ethyl acetate. The ethyl acetate phase was washed with water and saturated NaCl solution and, after removal of the solvent, the residue was purified by column chromatography (CH2Cl2/ethyl acetate). There were obtained 0.43 g of 3-[2-(5,5-dimethyl-[1,3]dioxan-2-yl)-4,5-dimethoxy-phenyl]-5-methyl-[1,2,4]oxadiazole as a white solid; MS: 334 ([M]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476264B2
Source datasetuspto-grants-2002_11
ORD IDord-72787124d54a4d92b84f9576768179ca
Source noteuspto-grants-2002_11