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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53200Generated: October 25, 2026

Sodium borohydride → Ethyl 3-(2-chloropyridin-5-yl)propionate

https://huagongshe.com/reaction/53200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-Ethyl 3-(6-chloropyridin-3-YL)acrylateHCID 53406713—
SolventEthanolHCID 702—
ProductEthyl 3-(2-chloropyridin-5-yl)propionateHCID 1908202084%

Reaction Steps

A suspension of 0.84 g (1 eq) of Te powder and 0.6 g (2 eq) of NaBH4 in 32 ml of ethanol was heated under nitrogen until it became a homogeneous purple solution. To the above hot solution was added ethyl β-(2-chloropyridin-5yl)acrylate (1.38 g, 6.5 mmol) and the mixture was refluxed for 4 h. The crude product was purified by flash chromatography (silica gel; hexane/ethyl acetate, 3:1) to afford 1.11 g (84,6%) of ethyl 3-(2-chloropyridin-5-yl)propionate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618821
Source datasetuspto-grants-1997_04
ORD IDord-ec542c1c9b2a40199ac51be469a0f6be
Source noteuspto-grants-1997_04