HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42849Erstellt: 25. Oktober 2026
Nitrogen → Ethyl 2-(hydroxymethyl)oxazole-4-carboxylate
https://huagongshe.com/reaction/42849
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitrogen | HCID 947 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Ethyl 2-formyl-1,3-oxazole-4-carboxylate | HCID 10583255 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 2-(hydroxymethyl)oxazole-4-carboxylate | HCID 10511369 | — |
Reaktionsschritte
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), 2-formyl-oxazole-4-carboxylic acid ethyl ester (272 mg, 1.61 mmol) was dissolved in EtOH (5.0 mL). NaBH4 (112 mg, 2.84 mmol) was added portionwise at 0° C. and the reaction mixture stirred at 0° C. for 1 h. Sat. aq. NH4Cl was added and the mixture extracted with EA (5×10 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a yellow oil. TLC: rf (EA)=0.50. LC-MS-conditions 02: tR=0.58 min; [M+H]+=172.03.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536209B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-7574e653ce0242f88265626ee61f4128 |
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| Quellennotiz | uspto-grants-2013_09 |
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