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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | 1,3-Thiazole-5-carbaldehyde | HCID 2773577 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59683351 | HCID 59683351 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371331B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-d5e777409d7b488c93c15dc6e09e158b |
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| Source note | uspto-grants-2016_06 |
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