HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368455Generated: October 25, 2026
Dichloromethane → 2-(3-Chloro-2,5,6-trifluoropyridin-4-yl)-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/368455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Chloro-2,4,5,6-tetrafluoropyridine | HCID 137183 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(3-Chloro-2,5,6-trifluoropyridin-4-yl)-1H-isoindole-1,3(2H)-dione | HCID 22121201 | 102.6% |
Reaction Steps
To a mixed solution of 40 ml dichloromethane and 20 ml N,N-methylformamide were added 18.5 g of 3-chloro-2,4,5,6-tetrafluoropyridine and 20.5 g potassium phthalimide, and the mixture was stirred at 40° C. for one day. After adding 40 ml of chloroform, the mixture was washed twice with 500 ml of distilled water and once with 500 ml of 0.5% aqueous solution of sodium hydroxide. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The precipitate was dispersed in diisopropylether, and collected by filtration to obtain 32.0 g of the title compound as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06133284 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-c6e8ca0371a344e8b40cc21463dd53a9 |
|---|
| Source note | uspto-grants-2000_10 |
|---|