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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380292Generated: November 2, 2026

Methane → 1'-[4-Bromo-2-fluorobenzyl]-7'-chloro-spiro[imidazolidine-4,3'-indoline]-2,2',5-trione

https://huagongshe.com/reaction/1380292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantEthanolHCID 702—
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium CarbonateHCID 517111—
Reactant1-[(4-Bromo-2-fluorophenyl)methyl]-7-chloro-1H-indole-2,3-dioneHCID 13248082—
SolventWaterHCID 962—
Product1'-[4-Bromo-2-fluorobenzyl]-7'-chloro-spiro[imidazolidine-4,3'-indoline]-2,2',5-trioneHCID 13691146—

Reaction Steps

A stirred suspension of 1-(4-bromo-2-fluorobenzyl)-7-chloro-indoline-2,3-dione (96 g.) in ethanol (1500 ml.) was treated with a solution of potassium cyanide (21.0 g.) and ammonium carbonate (300 g.) in water (1500 ml.). The mixture was stirred at 45°-50° C. for 4 hours. Activated charcoal (50 g.) was added and the mixture was stirred for a further hour at 45°-50° C. The hot mixture was filtered through diatomaceous earth and the filter cake was washed with aqueous ethanol (2×200 ml.; 1:1 v/v) at 60° C. The cooled filtrate was made acid to pH 4 at 0°-5° C. with 10M hydrochloric acid and the precipitated solid was collected by filtration, washed with water and air-dried. Recrystallisation twice from 1:1 v/v ethyl acetate-petrol 60-80 gave (±)-1'-(4-bromo-2-fluorobenzyl)-7'-chloro-spiro[imidazolidine-4,3'-indoline]-2,2',5-trione(60 g.) m.p. 240°-242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581366
Source datasetuspto-grants-1986_04
ORD IDord-34fecb9f09414a95afb6c654145ac7bc
Source noteuspto-grants-1986_04