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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749815Generated: November 1, 2026

Acetic Acid → 6-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde

https://huagongshe.com/reaction/1749815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHexamethylenetetramineHCID 4101—
ReactantSodium BicarbonateHCID 516892—
Reactant6-phenyl-1H-pyrrolo[2,3-b]pyridineHCID 86681999—
SolventWaterHCID 962—
Product6-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehydeHCID 8668200011%

Reaction Conditions

Temperature120 °C

Reaction Steps

6-Phenyl-1H-pyrrolo[2,3-b]pyridine (0.10 g, 0.52 mmol) was successively added with acetic acid (0.2 mL), water (0.4 mL), and hexamethylenetetramine (0.11 g, 0.77 mmol), and then the mixture was stirred overnight at 120° C. in a sealed tube. The reaction mixture was cooled to room temperature, and then added with saturated aqueous sodium hydrogencarbonate, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography (eluted with chloroform/methanol (99:1→99:5)) to obtain a solid containing the objective substance. The solid was washed with a mixed solvent of chloroform and methanol to obtain 6-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde (0.013 g, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-da0f7810a96d404db5f28814f6ed8609
Source noteuspto-grants-2015_10