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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30894Erstellt: 24. Oktober 2026

Methyl iodide → 6-Methyl-2-(methylsulfanyl)-1,3-benzoxazole

https://huagongshe.com/de/reaction/30894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt6-Methyl-1,3-benzoxazole-2-thiolHCID 963501—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Methyl-2-(methylsulfanyl)-1,3-benzoxazoleHCID 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, 1H), 7.20 (s, 1H), 7.10 (d, 1H), 2.78 (s, 3H), 2.42 (s, 3H); LC-MS ret. time 2.90 min (method 2), m/z 180.1 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423156B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-700388a930fb4a72add2bf9a78aeb928
Quellennotizuspto-grants-2008_09