HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 917388Erstellt: 26. Oktober 2026
Ethyl 2-chloroacetoacetate → Ethyl 2-anilino-4-methyl-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/917388
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Edukt | Phenylthiourea | HCID 676454 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 2-anilino-4-methyl-1,3-thiazole-5-carboxylate | HCID 807772 | 91,5% |
Reaktionsschritte
To 70 ml of ethanol, 10.7 g (70 mmol) of phenylthiourea and 11.6 g (70 mmol) of ethyl 2-chloro-3-oxobutanate were dissolved, followed by heating under refluxing for 8 hours. The reaction liquid was concentrated and dissolved in ethyl acetate and the organic layer was washed with an aqueous solution of sodium carbonate, water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure. Solid obtained was washed with diisopropyl ether to obtain 16.8 g (yield: 91%) of ethyl 4-methyl-2-(N-phenylamino)thiazole-5-carboxylate. (2) To 50 ml of ethanol, 12.8 g (49 mmol) of ethyl-4-methyl-2-(N-phenylamino)thiazole-5-carboxylate was dissolved, followed by adding 24 g (150 mmol) of 25% sodium hydroxide aqueous solution, and stirring at 80° C. for 15 hours. The reaction liquid was poured into ice water, and acetic acid was added to make acidic. Crystal precipitated was filtered, washed with water and a mixed solvent of hexane/ethyl acetate and dried to obtain 5.50 g (yield: 48%) of 4-methyl-2-(N-phenylamino)thiazole-5-carboxylic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07273878B2 |
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| Quelldatensatz | uspto-grants-2007_09 |
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| ORD ID | ord-6f9ad1ae7dd8467e9631e333a8a5a164 |
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| Quellennotiz | uspto-grants-2007_09 |
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