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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| 반응물 | (((1,3-Dibromopropan-2-yl)oxy)methyl)benzene | HCID 561824 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | [[[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy]methyl]Benzene | HCID 13298802 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08420629B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-cef10a2d79b84909a97b64b11bcc95c9 |
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| 출처 메모 | uspto-grants-2013_04 |
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