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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707018Generated: October 29, 2026

Triisopropylsilyl chloride → 5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/707018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 24229223—

Reaction Steps

To a mixture of 5-bromo-1H-pyrrolo[2,3-b]pyridine (15.4 g) in tetrahydrofuran (250 mL) was added 1M lithium hexamethyldisilazide in tetrahydrofuran (86 mL), and after 10 minutes, TIPS-Cl (triisopropylchlorosilane) (18.2 mL) was added. The mixture was stirred at room temperature for 24 hours. The reaction was diluted with ether, and the resulting solution was washed twice with water. The extracts were dried (Na2SO4), filtered, and concentrated. The crude product was chromatographed on silica gel with 10% ethyl acetate/hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174982B2
Source datasetuspto-grants-2015_11
ORD IDord-220318892e3e488dbd7a8d099aa3a397
Source noteuspto-grants-2015_11