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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301908Generated: October 30, 2026

Tetrafluorophthalic anhydride → (R)-2-(1-phenylethyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3-dione

https://huagongshe.com/reaction/2301908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluorophthalic anhydrideHCID 69545—
Reactant1-Phenethylamine, (+)-HCID 643189—
SolventChloroformHCID 6212—
Product(R)-2-(1-phenylethyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3-dioneHCID 46498665.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

220 mg of tetrafluorophthalic anhydride and 121 mg of (R)-α-methylbenzylamine were charged in an egg-plant type flask of 50 ml, followed by stirring under heating at a temperature of 180° C. for 2 hours. After cooled, the reaction product was dissolved in chloroform, purified by silica gel column chromatography (eluent; methylene chloride:methanol=30:1 v/v), recrystallized from a mixed solvent of n-hexane-ethyl acetate, to obtain 210 mg of the desired product as colorless needles. Yield: 65%. m.p. 95.5-96° C.; [α]20D=41.5° (C=0.348 AcOEt); MS(EI+) 323(M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06429212B1
Source datasetuspto-grants-2002_08
ORD IDord-de26b19b194d40d1a00e539cb2c2c519
Source noteuspto-grants-2002_08