HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1445758Erstellt: 26. Oktober 2026
Iodine → 2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazole
https://huagongshe.com/reaction/1445758
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol | HCID 10880530 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazole | HCID 58951394 | — |
Reaktionsschritte
Add iodine (1.90 g, 7.49 mmol) to a stirred mixture of 2-[2-(4-bromo-phenyl)-5-methyl-oxazol-4-yl]-ethanol (1.503 g, 5.33 mmol), triphenylphosphine (2.101 g, 8.01 mmol), and pyridine (1.4 mL, 17 mmol) in toluene (48 mL) and heat at 100° C. for 45 min. Cool to room temperature, add ethyl acetate and water, and separate the layers. Extract the aqueous layer twice with ethyl acetate, wash the organic layer with 0.1N HCl, dry over anhydrous magnesium sulfate, and concentrate under reduced pressure. Purify the residue by flash chromatography (SiO2, elute 0% to 10% EtOAc/hexanes) to-yield 1.804 g of the title compound as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.89 (d, J=8.4 Hz, 2H), 7.60 (d, J=8.8 Hz, 2H), 3.49 (dd, J=7.2, 7.2 Hz, 2H), 3.11 (dd, J=7.2, 7.2 Hz, 2H), 2.39 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07666871B2 |
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| Quelldatensatz | uspto-grants-2010_02 |
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| ORD ID | ord-ceb9f050bd8e44138dbb19c5551d1f16 |
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| Quellennotiz | uspto-grants-2010_02 |
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