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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-[2-(1H-indol-3-yl)ethyl]-1H-Isoindole-1,3(2H)-dione | HCID 288577 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(2-bromo-1H-indol-3-yl)-ethyl]-isoindole-1,3-dione | HCID 10970654 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849764 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-dba07d8d1aad4aa9b24f664fc1e04c77 |
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| Source note | uspto-grants-1998_12 |
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