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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1966170생성일: 2026년 10월 25일

Methyl (methylsulfinyl)methyl sulfide → [[[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy]methyl]Benzene

https://huagongshe.com/reaction/1966170

반응식

참여 물질

역할이름HCID투입량
반응물Methyl (methylsulfinyl)methyl sulfideHCID 99129—
반응물(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
반응물ButyllithiumHCID 178418339—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물[[[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy]methyl]BenzeneHCID 1329880256%

반응 단계

2.5 M of n-butyllithium in hexane (19 mL) was added to a solution of (methylsulfinyl)(methylthio)methane (5.0 g, 0.040 mol) in THF (10 mL) dropwise at −10° C. and the mixture was stirred for 3 h. To the resultant solution was added dropwise [2-bromo-1-(bromomethyl)ethoxy]methylbenzene (4.9 g, 0.016 mol) at −70° C. over 30 min. The mixture was stirred at this temperature for 3 h and then at rt over night. The reaction was diluted with dichloromethane and washed with water. The aqueous phases were extracted with dichloromethane. The organic layers were combined, washed with brine, dried over MgSO4, concentrated and purified with Combiflash (silica gel, 0-55% EtOAc/Hex) to give the desired product (2.4 g, 56%) as brown oil. LCMS (M+Na) 293.3. 1H NMR (400 MHz, CDCl3): δ 7.30 (5H, m), 4.45 (2H, s), 4.33 (1H, m), 2.75 (2H, m), 2.65 (2H, m), 2.41 (3H, s), 2.12 (3H, s) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08420629B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-cef10a2d79b84909a97b64b11bcc95c9
출처 메모uspto-grants-2013_04