HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 731171Erstellt: 25. Oktober 2026
1,3-Oxazole-2-carboxaldehyde → HCID 59855140, Verbindung
https://huagongshe.com/reaction/731171
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,3-Oxazole-2-carboxaldehyde | HCID 14786609 | — |
| Edukt | HCID 178419637 | HCID 178419637 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 59855140 | HCID 59855140 | — |
Reaktionsschritte
4-(2-Tetrahydro-3-H-pyranoxy)phenylmagnesium bromide (6.7 mmol) in THF (0.5 M) was added dropwise to a solution of oxazole-2-carbaldehyde (5.15 mmol) in THF (8 mL). After it was stirred at room temperature for 2.5 hours, the reaction was quenched with water and extracted with EtOAc (200 mL). The organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was column chromatographed (silica gel, 1:2 EtOAc/hexane). Compound M11.1 was obtained. MS ESI (pos.) m/e:276 (M+H). 1H NMR (400 MHz) (DMSO-d6) δ 8.02 (s, 1H); 7.31 (d, J=8.7 Hz, 2H); 7.14 (s, 1H); 6.97-7.01 (m, 2H); 6.27 (d, J=5 Hz, 1H); 5.74 (d, J=5 Hz, 1H); 5.44 (s, 1H); 3.74 (m, 1H); 3.52 (M, 1H); 1.72-1.81 (m, 3H); 1.52-1.60(m, 4H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582803B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-acb326583f6a446885ad4ae9dba9e2bd |
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| Quellennotiz | uspto-grants-2009_09 |
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