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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 549665Erstellt: 24. Oktober 2026

Methyl iodide → 5-Chloro-2-(methylsulfinyl)benzo[d]oxazole

https://huagongshe.com/de/reaction/549665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
EduktSodium ThiosulfateHCID 24477—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt5-Chloro-2-mercaptobenzoxazoleHCID 708870—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Chloro-2-(methylsulfinyl)benzo[d]oxazoleHCID 59671504—

Reaktionsschritte

Iodomethane (1.35 mL, 21.6 mmol) was added to a mixture of 5-chlorobenzo[d]oxazole-2(3H)-thione (2.00 g, 10.8 mmol) and K2CO3 (2.99 g, 21.6 mmol) in THF (43 mL). After 2 h, the reaction mixture was filtered and concentrated under reduced pressure. The crude material was dissolved in CH2Cl2 (40 mL) and meta-chloroperbenzoic acid (50-55%, 3.73 g, 10.8 mmol) was added at 0° C. The reaction was allowed to warm to rt. After stirring overnight, the reaction mixture was diluted with sodium thiosulfate (saturated, aqueous) and the organics were separated. The organics were washed with NaHCO3 (saturated, aqueous, 50 mL) and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. This gave 3.32 g (>100% crude yield) of the desired product as an orange solid. The material was used without further purification. LC-MS: RT=6.60 min., [M+H]+=216.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943622B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-58fcbe2642df4db5a2bf4b62d2f1c710
Quellennotizuspto-grants-2011_05