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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39415생성일: 2026년 10월 23일

Dimethyl Disulfide → 2-Methoxy-6-methylsulfanyl-4-trifluoromethyl-benzoic acid

https://huagongshe.com/ko/reaction/39415

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl DisulfideHCID 12232—
반응물2-Methoxy-4-(trifluoromethyl)benzoic acidHCID 3690873—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
생성물2-Methoxy-6-methylsulfanyl-4-trifluoromethyl-benzoic acidHCID 5919792111.1%

반응 단계

N,N,N′N′-Tetramethylethylendiamine (21 g, 177 mmol) was added drop-wise at −70° C. to a solution of sec-butyllithium (110 mL, 1.4 M in cyclohexane, 154 mmol) in 180 mL tetrahydrofuran. 2-Methoxy-4-trifluoromethyl-benzoic acid (13 g, 59 mmol) in 60 mL tetrahydrofuran was added drop-wise at −70° C. over 2 hours. After complete addition stirring was continued at −70° C. for another 2 hours. Dimethyl disulfide (20 g, 207 mmol) was added at −70° C. within 10 min. Stirring was continued at −70° C. for another hour and the reaction was allowed to warm up. The reaction mixture was quenched with 150 mL water and extracted with 200 mL ethyl acetate. The aqueous phase was adjusted to pH1 by addition of 25% HCl and extracted twice with dichloromethane. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The crude product was crystallized with heptane and yielded the title compound as a white solid (1.75 g, 11%), MS: m/e=265.1 [(M−H)−].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524909B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cfeddf249152461fb69082a9f0fec78e
출처 메모uspto-grants-2013_09