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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16393Generated: October 25, 2026

Acetic Anhydride → HCID 178434282, compound

https://huagongshe.com/reaction/16393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2',6'-DihydroxyacetophenoneHCID 69687—
SolventAcetic AcidHCID 176—
ProductHCID 178434282HCID 178434282—

Reaction Conditions

Temperature110 °C

Reaction Steps

526 mg (10.5 mmol) of hydrazine hydrate and 1 ml of glacial acetic acid are added to 800 mg (5.26 mmol) of 2,6-dihydroxyacetophenone. After 15 minutes of stirring at 110° C., the reaction mixture is cooled to room temperature. After addition of 6 ml of polyphosphoric acid, the mixture is heated at 120° C. for 20 min. After cooling to room temperature, 0.8 g (7.89 mmol) of acetic anhydride is added dropwise. The mixture is once more heated at 120° C. for 20 min. The reaction mixture, cooled to room temperature, is then poured onto ice. The mixture is neutralized using 1N sodium hydroxide solution and extracted three times with ethyl acetate. The combined organic phases are washed twice with water. After drying over sodium sulfate, the solvent is removed under reduced pressure. The product is purified by column chromatography. The mobile phase used is a mixture of cyclohexane and ethyl acetate (1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737153B2
Source datasetuspto-grants-2010_06
ORD IDord-4693e4e9fd814be5a66687e63f04c1e2
Source noteuspto-grants-2010_06