HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(4-Bromo-2-fluorobenzyl)-7-trifluoromethylindoline-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Trifluoromethylisatin | HCID 604575 | — |
| Reactant | 4-Bromo-2-fluorobenzyl bromide | HCID 2733660 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Bromo-2-fluorobenzyl)-7-trifluoromethylindoline-2,3-dione | HCID 13251292 | — |
Reaction Steps
Anhydrous potassium carbonate (10.7 g.) and 7-trifluoromethyl indoline-2,3-dione (14.4 g.) were stirred in N,N-dimethylformamide (DMF) (100 ml.) for 30 minutes. A portion (78.9 ml.) of a 25% w/v solution of 4-bromo-2-fluorobenzyl bromide in chlorobenzene was then added and the mixture was stirred at 75°-78° C. for 2 hours. The mixture was then cooled to ambient temperature and poured into water (400 ml.). Petrol 60-80 (200 ml.) was added to the aqueous mixture and the whole was stirred for 30 minutes. The solid which formed was separated by filtration to give 1-(4-bromo-2-fluorobenzyl)-7-trifluoromethyl indoline-2,3-dione (17.8 g.), m.p. 141°-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539329 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-cd230b9a548f42d9853ad6b52df645d4 |
| Source note | uspto-grants-1985_09 |