HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983002Generated: October 30, 2026
Sodium Hydroxide → HCID 22561694, compound
https://huagongshe.com/reaction/983002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromoindole | HCID 676494 | — |
| Reactant | 2-Chlorophenylboronic acid | HCID 2734322 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22561694 | HCID 22561694 | 38% |
Reaction Steps
To a mixture of 4-bromoindole (5.5 g, 28 mmol), and 2-chlorophenylboronic acid (4.4 g, 28 mmol) in THF (96 mL) were added Palladium catalyst Pd(PPh3)4 (0.975 g, 0.8 mmol) and the freshly prepared sodium hydroxide solution (3.4 g, 84 mmol in 40 mL of water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 75° C. oil bath for overnight. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed with brine, and dried over Na2SO4. After filtration, the solvents were evaporated, and the crude product was purified by a silica gel column to give 2.41 g (38%) of 4-(2-chloro-phenyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06861418B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-9c8d24487c3f478a89588e6a1bdb995b |
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| Source note | uspto-grants-2005_03 |
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