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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109294Generated: October 30, 2026

Acetic Anhydride → HCID 54381255, compound

https://huagongshe.com/reaction/1109294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54378503HCID 54378503—
SolventPyridineHCID 1049—
ProductHCID 54381255HCID 5438125584%

Reaction Steps

To a solution of 1-(N-hydroxy-N-methylcarbamoyl)-3-(3,5-di-tert-butyl-4-hydroxybenzylidene)pyrrolidin-2-one (Ia-6) (222 mg, 0.6 mmole) dissolved into pyridine (3 ml), 1.8 ml of acetic anhydride was added and the mixture was stirred at room temperature for 5 hours, then the resulting mixture was evaporated. Hydrochloric acid (0.5N) was added thereto, and the mixture was subjected to extraction with dichloromethane. The organic layer was washed with water, sodium bicarbonate, and water in order, dried over magnesium sulfate, and evaporated. The obtained residue was recrystallized from dichloromethane/ether, whereby 211 mg of the objective compound (Ia-16) was obtained in 84% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319100
Source datasetuspto-grants-1994_06
ORD IDord-648752adde114c55b5b85f46c8c823ca
Source noteuspto-grants-1994_06