HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52715Generated: October 26, 2026
Ethyl Acetate → 2-(N,N-Diethylamino)-4-(hydroxymethyl)thiazole
https://huagongshe.com/reaction/52715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Ethyl 2-(diethylamino)-1,3-thiazole-4-carboxylate | HCID 12966399 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(N,N-Diethylamino)-4-(hydroxymethyl)thiazole | HCID 18758970 | 73.9% |
Reaction Steps
A solution of 3.14 ml of lithium aluminum hydride in toluene was diluted in a dry flask under N2 atmosphere with 30 ml of THF. The resulting mixture was cooled to 0° C. and treated dropwise with a solution of 1.43 g (6.28 mmol) of ethyl 2-(N,N-diethylamino)thiazole-4-carboxylate in 5 ml of THF. After addition, the solution was allowed to warm slowly to ambient temperature, stirred for 1 h, recooled to 0° C., and treated with a small amount of aqueous Rochelle's salt followed by ethyl acetate. After stirring, the slurry was filtered, washed with additional ethyl acetate, and the combined filtrates were concentrated in vacuo. The residue was purified by silica gel chromatography using methanol in chloroform to provide 0.864 g (73%) of the desired compound, Rf 0.17 (4% methanol in chloroform). Mass spectrum: (M+H)+ =187.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616720 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-b0d75e6ee67840ea8b4ff5b07709fc98 |
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| Source note | uspto-grants-1997_04 |
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