돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70128생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물Sodium ThiosulfateHCID 24477—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물5-Chloro-2-mercaptobenzoxazoleHCID 708870—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-2-(methylsulfinyl)benzo[d]oxazoleHCID 59671504—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822472B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-67a4d463a2254d9da7ab82d6208349dd
출처 메모uspto-grants-2014_09