HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446409Generated: October 29, 2026
Ethyl bromopyruvate → Ethyl 2-ethyl-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/446409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Propanethioamide | HCID 2760628 | — |
| Reactant | 2-(2-Chloro-5-(hydroxymethyl)phenyl)ethanol | HCID 57989337 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-ethyl-1,3-thiazole-4-carboxylate | HCID 15056276 | — |
Reaction Steps
Ethyl 3-bromo-2-oxopropanoate (24.7 mL) was added dropwise over 10 min to a solution of propanethioamide [Carboxylic Acid 1, step a] (15.8 g) in ethanol (150 mL) at 0-10° C. under nitrogen. When the addition was complete the mixture was stirred at ambient temperature for 18 hours. The mixture was concentrated in vacuo, the residue diluted with water and extracted into ethyl acetate (×3). The combined extracts were washed with brine, dried over magnesium sulfate, filtered and the solvent removed. The crude product was purified by flash silica chromatography, elution gradient 10, 15 and 20% ethyl acetate in isohexane. Fractions containing the product were evaporated to dryness to afford the subtitled compound as a pale green solid. Yield 16.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6bf56635758548ac98369446656d35ab |
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| Source note | uspto-grants-2013_07 |
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