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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285536Generated: October 31, 2026

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

https://huagongshe.com/reaction/1285536

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 13248082—

Reaction Steps

A suspension of 7-chloroindoline-2,3-dione (15g.) 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 10 M 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 numberUS04567278
Source datasetuspto-grants-1986_01
ORD IDord-d475c6ff1b0e43c3855c4b892140c324
Source noteuspto-grants-1986_01