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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747540Generated: October 30, 2026

Ethyl orthoformate → HCID 58079761, compound

https://huagongshe.com/reaction/1747540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthanolHCID 702—
ProductHCID 58079761HCID 5807976192.2%

Reaction Steps

In ethanol (60 mL) was dissolved 6-bromonicotinaldehyde (2.00 g, 10.8 mmol). Triethyl orthoformate (5.37 mL, 32.3 mmol) and p-toluenesulfonic acid monohydrate (102 mg, 0.538 mmol) were added and the mixture was refluxed for 2 hours. The solvent in the reaction mixture was evaporated under reduced pressure, and a saturated aqueous sodium bicarbonate solution and water were added. Extraction with ethyl acetate, washing with saturated brine and drying over anhydrous sodium sulfate were performed. After filtration, the solvent in the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1) to give 2-bromo-5-(diethoxymethyl)pyridine (2.59 g, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150569B2
Source datasetuspto-grants-2015_10
ORD IDord-34323a20311840a787260d0b85cfb50e
Source noteuspto-grants-2015_10