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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356313Generated: October 29, 2026

Acetic acid, azido-, ethyl ester → Ethyl 2-azido-3-(2-chloropyridin-3-yl)-3-hydroxypropionate

https://huagongshe.com/reaction/356313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant2-Chloro-3-pyridinecarboxaldehydeHCID 737607—
ReactantSodium ethoxideHCID 2723922—
SolventWaterHCID 962—
ProductEthyl 2-azido-3-(2-chloropyridin-3-yl)-3-hydroxypropionateHCID 2329827874%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2.0 g of 2-chloro-3-formylpyridine (prepared as described in Preparation 75), 7.5 g of ethyl azidoacetate and 87 ml of a 65 mM ethanolic solution of sodium ethoxide was stirred at 0° C. for 2 hours. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride, in that order, and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 3:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 2.83 g of the title compound having Rf=0.61 (on silica gel thin layer chromatography using a 2:1 by volume mixture of hexane and ethyl acetate as the developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834501
Source datasetuspto-grants-1998_11
ORD IDord-6433c1ab5d694cd08480efd81885d325
Source noteuspto-grants-1998_11