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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266703Generated: November 2, 2026

Acetic Anhydride → HCID 54564406, compound

https://huagongshe.com/reaction/266703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54527172HCID 54527172—
SolventPyridineHCID 1049—
ProductHCID 54564406HCID 5456440680%

Reaction Steps

To a cooled solution of N-phenyl β-(4-hydroxy-5,6,7,8-tetrahydronaphth-1-yl)-α-cyanoacrylamide (3.184 g, 0.010 mol) in dry pyridine (5 ml) was added acetic anhydride (2.040 g, 0.020 mol) and the mixture maintained at 0°-5° C. overnight. Thereupon the mixture was concentrated under vacuum, the residue dissolved in dichloromethane, the organic layer washed with water and then evaporated under reduced pressure. The crude product was crystallized from chloroform/methanol to yield pure title compound in about 80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652250
Source datasetuspto-grants-1997_07
ORD IDord-ab19fcfc082c40c3a3a4d157484b18d1
Source noteuspto-grants-1997_07