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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30894생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물6-Methyl-1,3-benzoxazole-2-thiolHCID 963501—
용매TetrahydrofuranHCID 8028—
생성물6-Methyl-2-(methylsulfanyl)-1,3-benzoxazoleHCID 21985788—

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423156B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-700388a930fb4a72add2bf9a78aeb928
출처 메모uspto-grants-2008_09