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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702649Generated: October 29, 2026

Acetic Anhydride → HCID 15580725, compound

https://huagongshe.com/reaction/1702649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15580713HCID 15580713—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 15580725HCID 15580725—

Reaction Steps

A mixture of 8.0 g. of 3-amino-1-(p-chlorophenyl)-5-methyl-2-pyrazoline (prepared as described in Example 20), 400 mg. of 4-dimethylaminopyridine and 20.0 ml. of acetic anhydride is allowed to stand at room temperature for 48 hours. The solid formed is collected by filtration, washed with cold acetic anhydride, then with hexane and is dried to give a white solid. The solid is recrystallized from dichloromethane-hexane to give 6.6 g. of the product of the Example as a white solid, m.p. 167°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348527
Source datasetuspto-grants-1982_09
ORD IDord-587f831cc8c246f09d7eccaddc61f7bd
Source noteuspto-grants-1982_09