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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
Reactantethyl 7-bromo-3-(3-hydroxypropyl)-1H-indole-2-carboxylateHCID 68943187—
SolventDichloromethaneHCID 6344—
Productethyl 7-bromo-3-(3-iodopropyl)-1H-indole-2-carboxylateHCID 68936016—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359296B2
Source datasetuspto-grants-2016_06
ORD IDord-baa1b37142d74358932350dd1f810e7a
Source noteuspto-grants-2016_06