HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252488Generated: October 27, 2026
Iodine → 1-ethyl-2-iodo-6-methoxy-1H-indole-3-carbonitrile
https://huagongshe.com/reaction/252488
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-ethyl-6-methoxy-1H-indole-3-carbonitrile | HCID 11644100 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-ethyl-2-iodo-6-methoxy-1H-indole-3-carbonitrile | HCID 59425644 | 62% |
Reaction Steps
A 2M solution of lithium diisopropyl amide in THF/hexanes (Acros) (3.9 mL, 7.8 mmol) is diluted with THF (5 mL) in a flame-dried flask. After cooling the reaction to −30° C., a solution of 1-ethyl-6-methoxy-1H-indole-3-carbonitrile (1.30 g, 6.5 mmol) in THF (10 mL) is added dropwise during 10 min, maintaining the temperature at −30° C. After stirring for an additional 30 min at this temperature, a solution of iodine (2.31 g, 9.1 mmol) in THF (5 mL) is added during 10 min. After the addition, the reaction is warmed to ambient temperature during 1 h. The reaction is then diluted with ice-H2O and extracted with EtOAc (2×). The combined organic phases are washed with 1M sodium thiosulfate and saturated NaCl and then concentrated to a brown solid. Chromatography (CH2Cl2/hexanes, 1/1) over silica gel gives 1.31 g (62%) of 1-ethyl-2-iodo-6-methoxy-1H-indole-3-carbonitrile as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868037B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-bac93d07f5c8491aa0047354110b9583 |
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| Source note | uspto-grants-2011_01 |
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