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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250604Generated: October 25, 2026

Tetrabutylammonium Fluoride → methyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/250604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1-Triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl esterHCID 66679244—
SolventTetrahydrofuranHCID 8028—
Productmethyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 2283204960%

Reaction Steps

To 1-Triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester (531, 0.950 g, 2.9 mmol) in tetrahydrofuran (20.0 mL) was added tetrabutyl-ammonium fluoride, trihydrate (1.20 g, 3.8 mmol). The reaction was stirred at room temperature for 10 minutes. The reaction was concentrated and purified with silica gel column chromatography eluting with 4% methanol in methylene chloride to give the compound as a white solid (532, 300 mg, 60%). MS (ESI) [M+H+]+=177.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863288B2
Source datasetuspto-grants-2011_01
ORD IDord-be303498cdeb4158b4dffb0016e4a4db
Source noteuspto-grants-2011_01