HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593402Generated: November 1, 2026
1,2-Difluorobenzene → HCID 21905880, compound
https://huagongshe.com/reaction/1593402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Difluorobenzene | HCID 9706 | — |
| Reactant | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21905880 | HCID 21905880 | 43% |
Reaction Steps
A solution of 5.6 g of 1,2-difluorobenzene in 50 ml of ether is cooled to −10° C, 31 ml of a 1.6 M solution of n-butyllithium in hexane are added drop wise and the mixture is stirred at −10° C. for 2 hours. The reaction mixture is cooled to −50° C., a solution of 4 g of 5-chloro-1H-indole-2,3-dione in 40 ml of THF is added and the resulting mixture is stirred for 12 hours, while allowing the temperature to return to RT. The reaction mixture is poured into a concentrated HCl/ice/water mixture, the resulting mixture is extracted with EtOAc, the organic phase is washed with 1N NaOH solution, with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained after crystallization from iso-ether; m.p.=248° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07297692B2 |
|---|
| Source dataset | uspto-grants-2007_11 |
|---|
| ORD ID | ord-f920e2d7fcb9413b887b5bdb24f06eda |
|---|
| Source note | uspto-grants-2007_11 |
|---|