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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128013Generated: October 29, 2026

Acetic Anhydride → HCID 23471620, compound

https://huagongshe.com/reaction/128013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 23471618HCID 23471618—
SolventChloroformHCID 6212—
ProductHCID 23471620HCID 23471620—

Reaction Steps

To a solution of 5-(5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)indoline in 100 ml of chloroform was added 5 ml of triethylamine with stirring. To the mixture was added dropwise 3 ml of acetic anhydride. After maintaining at room temperature for one hour, the reaction mixture was concentrated under reduced pressure. The residual crystals were filtered off, washed with water and recrystallized from ethanol to give 4.3 g of 5-(5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1-acetylindoline as white crystals, melting at 258°-261° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04258185
Source datasetuspto-grants-1981_03
ORD IDord-244f7a2d20454e34933c5944740d6b15
Source noteuspto-grants-1981_03