HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1768525Erstellt: 26. Oktober 2026
Carbon Dioxide → 4-Cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acid
https://huagongshe.com/reaction/1768525
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | 2-Isopropyl-oxazole-4-carboxylic acid-cyclopropylamide | HCID 15672429 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 4-Cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acid | HCID 15672430 | 81% |
Reaktionsschritte
0.12 mol of n-butyllithium (80.0 ml of a 1.5 molar solution in hexane) was added dropwise to a solution of 10.4 g (0.054 mol) of 2-(1-methylethyl)-oxazole-4-carboxylic acid cyclopropylamide in 250 ml of tetrahydrofuran under a nitrogen atmosphere of -70° C. and stirring was carried out for 30 minutes at this temperature. Thereafter, the reaction mixture was poured onto 500 g of solid CO2 and was left to stand overnight. The mixture was evaporated down, the residue was taken up in 200 ml of water and 30 ml of 10% strength NaOH, the solution was extracted twice with diethyl ether and the aqueous phase was acidified to pH 2 with concentrated hydrochloric acid and extracted with ethyl acetate. The organic phase was dried with magnesium sulfate and the solvent was stripped off under reduced pressure. 10.4 g (81%) of 4-cyclopropylaminocarbonyl-2-(1-methylethyl)-oxazole-5-carboxylic acid were obtained as a white powder of melting point 109° -112° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05378680 |
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| Quelldatensatz | uspto-grants-1995_01 |
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| ORD ID | ord-5bde1ae0489f4953b2b8cb2e36f8a10e |
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| Quellennotiz | uspto-grants-1995_01 |
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