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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020936Generated: November 1, 2026

Acetic Anhydride → HCID 58371859, compound

https://huagongshe.com/reaction/1020936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178486231HCID 178486231—
ProductHCID 58371859HCID 58371859—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-bromo-N′-methylbenzimidohydrazide hydrochloride 1 (1.7 g) (prepared according to a procedure in synthesis of Sch-1499895) in acetic anhydride (10 ml) was heated at 100° C. for 0.5 hour. After cooling and concentration under reduced pressure, the residue was dissolved in EtOAc, washed with saturated NaHCO3 twice, brine and dried (MgSO4). After evaporation of solvent, the residue was purified on silica gel. Elution with EtOAc gave 3-(4-bromophenyl)-1,5-dimethyl-1H-[1,2,4]-triazole 2BK (1.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716483B2
Source datasetuspto-grants-2014_05
ORD IDord-656f3ea274ec4f639a79657aad1623b9
Source noteuspto-grants-2014_05