HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907096Generated: October 31, 2026
Iodine → 1-ethyl-2-iodo-6-methoxy-1H-indole-3-carbonitrile
https://huagongshe.com/reaction/907096
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) was 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) was 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) was added during 10 min. After the addition, the reaction was warmed to ambient temperature during 1 h. The reaction was then diluted with ice-H2O and extracted with EtOAc (2×). The combined organic phases were washed with 1M sodium thiosulfate and saturated NaCl and then concentrated to a brown solid. Chromatography (CH2Cl2/hexanes, 1/1) over silica gel gave 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 | US08013006B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-5444c5515bbd4a07b432a1696001153d |
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| Source note | uspto-grants-2011_09 |
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