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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022429Generated: November 2, 2026

Iodoethane → HCID 86704559, compound

https://huagongshe.com/reaction/1022429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dichloro-1H-pyrrolo[3,2-c]pyridineHCID 5358988—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86704559HCID 8670455969.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine (250 mg, 1.34 mmol) in tetrahydrofuran (4 mL) at 0° C. was treated with a 60% dispersion of sodium hydride in mineral oil (64.2 mg, 2.67 mmol) followed by iodoethane (229 mg, 1.47 mmol). After stirring at 0° C. for 0.5 h, the reaction mixture was allowed to warm to room temperature and was stirred at room temperature overnight. At this time, the resulting mixture was quenched with a saturated aqueous sodium bicarbonate solution. The reaction mixture was extracted with ethyl acetate. The combined organics were washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (30% ethyl acetate/hexane) afforded 4,6-dichloro-1-ethyl-1H-pyrrolo[3,2-c]pyridine (200 mg, 69.6%). LC-MS calcd. for C9H8Cl2N2 [(M)+] 214, obsd. 214.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722661B2
Source datasetuspto-grants-2014_05
ORD IDord-b07ad3f65a454ad9bc6d621bbc25a9c6
Source noteuspto-grants-2014_05