돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257145생성일: 2026년 10월 25일

Hydrochloric Acid → 7-Methoxymethylbenzo-1,2,3-thiadiazole

https://huagongshe.com/reaction/257145

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물1,2,3-Benzothiadiazol-7-ylmethanolHCID 20096433—
반응물HCID 178418361HCID 178418361—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물7-Methoxymethylbenzo-1,2,3-thiadiazoleHCID 20096427—

반응 단계

1.4 g of sodium hydride (50% dispersion in oil) in 15 ml of absolute dimethyl sulfoxide are introduced into a reaction vessel, and a solution of 4.15 g of 7-hydroxymethylbenzo-1,2,3-thiadiazole in 15 ml of tetrahydrofuran is added dropwise at 0°-5° C. under a nitrogen atmosphere and with stirring, during which process hydrogen is evolved. After 20 minutes of stirring at 10° C., the mixture is cooled down to 0°-5° C., and a solution of 4 g of methyl iodide in 15 ml of tetrahydrofuran is added dropwise. Stirring is continued for another hour at room temperature, and the mixture is cooled, treated with ice-water, neutralised with dilute hydrochloric acid and extracted with ethyl acetate. The extracts are washed with water, dried over sodium sulfate and evaporated, and the residue is dried in a high vacuum, resulting in the title compound in the form of a yellow oil, nD27 =1.5912.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260423
출처 데이터셋uspto-grants-1993_11
ORD IDord-573aec29607b4d85b5e99041ece57b30
출처 메모uspto-grants-1993_11