HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199725Generated: October 29, 2026
Imidazole → ethyl 7-bromo-3-(3-iodopropyl)-1H-indole-2-carboxylate
https://huagongshe.com/reaction/2199725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | ethyl 7-bromo-3-(3-hydroxypropyl)-1H-indole-2-carboxylate | HCID 68943187 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 7-bromo-3-(3-iodopropyl)-1H-indole-2-carboxylate | HCID 68936016 | — |
Reaction Steps
To a mixture of EXAMPLE 1B (1.116 g) in dichloromethane (30 mL) at 0° C. was added iodine (1.01 g), triphenyl phosphine (1.03 g) and imidazole (0.535 g). The mixture was stirred at 0° C. for 1 hour and treated with saturated NaHCO3 (50 mL). Stirring was continued for 30 minutes, and the organic layer was washed with a saturated aqueous Na2S2O3 (50 mL), water (20 mL), and brine (50 mL) and dried (Na2SO4), filtered and concentrated. The concentrate was purified by column chromatography on silica gel (with 0-20% ethyl acetate in hexanes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359296B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-baa1b37142d74358932350dd1f810e7a |
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| Source note | uspto-grants-2016_06 |
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