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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64955Generated: October 29, 2026

Hydrochloric Acid → 1-[(4-Bromo-2-fluorophenyl)methyl]-7-chloro-1H-indole-2,3-dione

https://huagongshe.com/reaction/64955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant7-ChloroisatinHCID 344135—
Reactant4-Bromo-2-fluorobenzyl bromideHCID 2733660—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventChlorobenzeneHCID 7964—
Product1-[(4-Bromo-2-fluorophenyl)methyl]-7-chloro-1H-indole-2,3-dioneHCID 1324808250.9%

Reaction Steps

A suspension of 7-chloroindoline-2,3-dione (15 g.) and potassium carbonate (15 g.) in N,N-dimethylformamide (100 ml.) was stirred and treated with a solution of 4-bromo-2-fluorobenzyl bromide (24.7 g.) in chlorobenzene (100 ml.). The mixture was stirred at 90° C. for five hours, cooled to ambient temperature, and diluted with a mixture of water (500 ml.) and petrol ether (b.p 60°-80° C.) (500 ml.) The aqueous phase was adjusted to pH3 with 10M hydrochloric acid. The mixture obtained was separated by filtration. The solid obtained was washed with further petrol ether, then with water, and recrystallised from ethanol to give 1-(4-bromo-2-fluorobenzyl)-7-chloro-indoline-2,3-dione (15.5 g.), m.p. 164°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04611062
Source datasetuspto-grants-1986_09
ORD IDord-2600c3531f164ac6aff29a8a7d681b69
Source noteuspto-grants-1986_09