Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711294Generated: October 31, 2026

Sodium hydride → 1H-Pyrrolo[2,3-b]pyridine-3-carboxaldehyde, 1-[[2-(trimethylsilyl)ethoxy]methyl]-

https://huagongshe.com/reaction/711294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
SolventDimethylformamideHCID 6228—
Product1H-Pyrrolo[2,3-b]pyridine-3-carboxaldehyde, 1-[[2-(trimethylsilyl)ethoxy]methyl]-HCID 9002352766%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1H-pyrrolo[2,3-B]pyridine-3-carbaldehyde (2.0 g, 13.7 mmol) in 20 mL DMF at 0° C. was added NaH (328 mg, 13.7 mmol). The suspension was allowed to stir at 0° C. for 30 min, then [2-(chloromethoxy)ethyl](trimethyl)silane (2.67 mL, 15.1 mmol) was slowly added. The reaction was allowed to warm to ambient temperature and stirred for 16 h. The mixture was concentrated and partitioned between saturated NaHCO3 and CH2Cl2. The organics were washed with water and brine, then dried over Na2SO4, filtered and concentrated. The crude solid was triturated with CH2Cl2 and filtered. The filtrate was concentrated and purified by silica gel chromatography (0-25% ethylacetate/hexanes) to give 1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (66%). LCMS [M+H]+=277.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181261B2
Source datasetuspto-grants-2015_11
ORD IDord-668c7a5bed6e472e91cf2d74472a5e9b
Source noteuspto-grants-2015_11