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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (R)-2-(1-phenylethyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3-dione | HCID 464986 | 65.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06429212B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-de26b19b194d40d1a00e539cb2c2c519 |
|---|
| Source note | uspto-grants-2002_08 |
|---|