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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518123Generated: November 3, 2026

Ammonium Chloride → Ethyl 2-azido-3-(5-methylthiophen-2-yl)acrylate

https://huagongshe.com/reaction/518123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Methyl-2-thiophenecarboxaldehydeHCID 61663—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodium ethoxideHCID 2723922—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductEthyl 2-azido-3-(5-methylthiophen-2-yl)acrylateHCID 7660191772.1%

Reaction Steps

To a solution of ethyl azidoacetate (10.6 g) in methanol (65 mL) was added sodium ethoxide (20% solution in ethanol, 27.2 g) under ice-cooling, and the mixture was stirred at the same temperature for 1 hour. 5-Methylthiophene-2-carbaldehyde (2.5 g) was added to this solution and the mixture was stirred at room temperature for 1 hour. To the reaction solution was added saturated ammonium chloride aqueous solution and water, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=100/0−90/10) to give the title compound (3.39 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115144B2
Source datasetuspto-grants-2015_08
ORD IDord-cc182f3ea8f94aaeb8e1da5b43927dd6
Source noteuspto-grants-2015_08