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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206569Generated: October 30, 2026

Acetic acid, azido-, ethyl ester → HCID 59683351, compound

https://huagongshe.com/reaction/2206569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant1,3-Thiazole-5-carbaldehydeHCID 2773577—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 59683351HCID 5968335123%

Reaction Steps

To a solution of thiazole-5-carbaldehyde (20 g, 176.77 mmol) and ethyl 2-azidoacetate (91.2 g, 707.1 mmol) in anhydrous ethanol (100 mL) was added sodium (16.26 g, 707.1 mmol) dissolved in anhydrous ethanol (1000 mL) dropwise between −10° C. and 0° C. After the addition, the mixture was stirred below 0° C. for 4 hours, and then warm to the ambient temperature and allowed to stir overnight. The reaction mixture was washed with saturated ammonium chloride, extracted with acetic ester (500 mL×3), the combined organic phase was dried by anhydrous sodium sulphate, and then filtered. The filtrate was concentrated and purified by column chromatograph on silica gel eluted with (petrol ether/acetic ester 20:1→10:1) to afford the title compound (9 g, 23%) as an yellow solid. LCMS (M+H+) m/z: calcd. 224.04. found 224.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-d5e777409d7b488c93c15dc6e09e158b
Source noteuspto-grants-2016_06