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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458333Generated: November 2, 2026

2-[2-(1H-indol-3-yl)ethyl]-1H-Isoindole-1,3(2H)-dione → 2-[2-(2-bromo-1H-indol-3-yl)-ethyl]-isoindole-1,3-dione

https://huagongshe.com/reaction/1458333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[2-(1H-indol-3-yl)ethyl]-1H-Isoindole-1,3(2H)-dioneHCID 288577—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(2-bromo-1H-indol-3-yl)-ethyl]-isoindole-1,3-dioneHCID 10970654—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[2-(1H-indol-3-yl)-ethyl]-isoindole-1,3-dione (1.0 g in a mixture of 10 mL dry tetrahydrofuran and 10 mL dry chloroform) at 0° C. was added pyridinium bromide perbromide (1.14 g) and the reaction stirred at 0° C. After 50 minutes, the reaction was quenched by the addition of saturated sodium bicarbonate and extracted with ethyl acetate. The organic portion was washed with saturated sodium bicarbonate (3x) and 0.3M sodium bisulfate (3x) then dried over magnesium sulfate. Purification of the concentrate by flash chromatography on silica gel (hexane:ethyl acetate, 3:1) gave the title compound (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849764
Source datasetuspto-grants-1998_12
ORD IDord-dba07d8d1aad4aa9b24f664fc1e04c77
Source noteuspto-grants-1998_12