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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352228Generated: October 30, 2026

Ethyl 2-bromo-2-(pyridin-3-yl)acetate → HCID 69848647, compound

https://huagongshe.com/reaction/352228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—
ReactantHCID 178418642HCID 178418642—
SolventDimethylformamideHCID 6228—
SolventSodiumHCID 5360545—
ProductHCID 69848647HCID 698486478%

Reaction Steps

The product was formed in a manner similar to preparation 396 using the in situ-generated sodium salt of the 4-hydroxypyridine (2.13 g; 18.2 mmol; 1.2 equiv) and an aliquot of bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 3.6 g; 15 mmol) in DMF (20 mL). Column chromatographic purification over SiO2 (1% methanol/chloroform) produced a yellow/orange oil (320 mg; approx. 8% yield). MS(ES) calc'd: [M+H]+=259.2 m/z. Pound: 259.1 m/z.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743794B2
Source datasetuspto-grants-2004_06
ORD IDord-f7f179a6ef874b2e980a7e2f78d4e6cf
Source noteuspto-grants-2004_06