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HRID 70128作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/70128

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物Sodium ThiosulfateHCID 24477—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物5-Chloro-2-mercaptobenzoxazoleHCID 708870—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-2-(methylsulfinyl)benzo[d]oxazoleHCID 59671504—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822472B2
出典データセットuspto-grants-2014_09
ORD IDord-67a4d463a2254d9da7ab82d6208349dd
出典メモuspto-grants-2014_09