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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719229Generated: October 27, 2026

Water → 1-(4-Bromo-2-fluorobenzyl)-7-trifluoromethylindoline-2,3-dione

https://huagongshe.com/reaction/1719229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant7-TrifluoromethylisatinHCID 604575—
Reactant4-Bromo-2-fluorobenzyl bromideHCID 2733660—
SolventDimethylformamideHCID 6228—
SolventChlorobenzeneHCID 7964—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-2-fluorobenzyl)-7-trifluoromethylindoline-2,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539329
Source datasetuspto-grants-1985_09
ORD IDord-cd230b9a548f42d9853ad6b52df645d4
Source noteuspto-grants-1985_09