HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9579Erstellt: 24. Oktober 2026
Methyl iodide → 6-Methyl-2-(methylsulfanyl)-1,3-benzoxazole
https://huagongshe.com/de/reaction/9579
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 6-Methyl-1,3-benzoxazole-2-thiol | HCID 963501 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-Methyl-2-(methylsulfanyl)-1,3-benzoxazole | HCID 21985788 | — |
Reaktionsschritte
6-Methyl-1,3-benzoxazole-2(3H)-thione (375 mg, 2.27 mmol) was dissolved in THF (2.0 mL), and iodomethane (1610.8 mg, 11.35 mmol) and potassium carbonate (627.36 mg, 4.54 mmol) were added. This reaction mixture was stirred vigorously at rt overnight. The reaction mixture was filtered and the solid was rinsed with additional THF. The filtrate was concentrated in vacuo to a yellow solid. The solid was partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried with MgSO4, and concentrated. The solid was dried for 1 h in a 50° C. oven. The product 6-methyl-2-(methylsulfanyl)-1,3-benzoxazole was obtained as yellow solid (145 mg, 35.6%). 1H NMR (300 MHz, DMSO-d6) δ 7.50 (d, 1 H), 7.20 (s, 1 H), 7.10 (d, 1 H), 2.78 (s, 3 H), 2.42 (s, 3 H); LC-MS ret. time 2.90 min (method 2), m/z 180.1 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091228B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-3262dfcd76f846518796ae0f5231d23d |
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| Quellennotiz | uspto-grants-2006_08 |
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