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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308715Generated: November 1, 2026

Acetic Anhydride → HCID 13957978, compound

https://huagongshe.com/reaction/2308715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13958012HCID 13958012—
ProductHCID 13957978HCID 13957978—

Reaction Steps

A mixture of 476 mg (2.0 mmole) of 3-(3-pyridylcarbonyl)-2-oxindole and 4 ml of acetic anhydride was heated under reflux for 30 minutes The reaction mixture was cooled to room temperature, the bulk of the acetic anhydride was removed by evaporation in vacuo and the residue was triturated under 15 ml of water. The solid was recovered by filtration, dried and triturated under isopropanol. The residue (158 mg) was recrystallized from acetonitrile giving 64 mg of the title compound as red-orange crystals, m.p. 142.5°-143.5° C. A second crop of title compound (40 mg) was obtained from the mother liquors from the recrystallization. The two crops were the same by thin-layer chromatography. The first crop was subjected to elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04690943
Source datasetuspto-grants-1987_09
ORD IDord-093c12ca4e0c44d9b746b17f5694f845
Source noteuspto-grants-1987_09