Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165237Generated: October 30, 2026

Acetic Anhydride → HCID 20098370, compound

https://huagongshe.com/reaction/1165237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 20098375HCID 20098375—
ProductHCID 20098370HCID 20098370—

Reaction Steps

A suspension of 2.6 g of the product of Step A in 70 ml of tetrahydrofuran was cooled to 0° to 5° C. and then 4.7 ml of acetic anhydride were added. The mixture was held at room temperature for 3 hours and was then evaporated to dryness under reduced pressure at 50° C. The residue was taken up in a 1-1 mixture of chloroform-methanol and was filtered. The product was dried at 80° C. to obtain 2.7 g of 5-acetylamino-2-acetoxy-N-(1H-indol-4-yl)-benzamide melting at 263° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908367
Source datasetuspto-grants-1990_03
ORD IDord-53b98cc2eea6445585a4beaaffcbf9d3
Source noteuspto-grants-1990_03