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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203742Generated: November 2, 2026

Sodium hydride → 4-Chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/2203742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 1143827299%

Reaction Steps

4-Chloro-1H-pyrrolo[2,3-b]pyridine (5.0 g, 32.8 mmol) in THF (50 mL) was cooled to 0° C., and NaH (1.64 g, 41.0 mmol, 60% oil dispersion) was added. After 15 minutes, triisopropylsilylchloride (“TIPS-Cl”; 6.94 mL, 32.8 mmol) was added, and the reaction was stirred at room temperature for 1 hour. A saturated ammonium chloride solution (20 mL) was added, and the mixture was extracted with hexanes (40 mL), washed with brine and dried over sodium sulfate. After removal of the solvent, the residue was purified by chromatography (hexanes) to give 4-chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine (10.0 g, 99% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-f9c581b4453440fe8828a95f3a3e1dc6
Source noteuspto-grants-2016_06