Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 748689생성일: 2026년 10월 25일
Diethylene glycol vinyl ether → 2-[1-[(4-Chlorophenyl)sulfonyl]-3-(2-vinyloxyethoxy)propyl]-1,4-difluorobenzene
https://huagongshe.com/reaction/748689
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethylene glycol vinyl ether | HCID 13581 | — |
| 반응물 | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| 반응물 | 2-(((4-Chlorophenyl)sulfonyl)methyl)-1,4-difluorobenzene | HCID 9901028 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-[1-[(4-Chlorophenyl)sulfonyl]-3-(2-vinyloxyethoxy)propyl]-1,4-difluorobenzene | HCID 59750768 | — |
반응 단계
In toluene (30 ml) was dissolved the 2-[(4-chlorophenyl)sulfonylmethyl]-1,4-difluorobenzene (520 mg, 1.72 mmol) obtained in Example 5. After addition of 2,2-(2-vinyloxyethoxy)ethanol (0.270 ml, 2.10 mmol) and cyanomethylenetri-n-butylphosphorane (500 mg, 2.07 mmol), the mixture was heated under reflux for 24 hours under an argon atmosphere. The reaction mixture was then allowed to cool down. After addition of 2-(2-vinyloxyethoxy)-ethanol (0.170 ml, 1.25 mmol) and cyanomethylenetri-n-butylphosphorane (300 mg, 1.24 mmol), the mixture was heated under reflux for 12 hours under an argon atmosphere. The reaction mixture was allowed to cool down and then concentrated under reduced pressure. The residue thus obtained was purified by silica gel chromatography (hexane:ethyl acetate=7:1) to yield a white solid. The resulting white solid was washed with hexane, whereby the title compound (140 mg, 20%) was obtained as a white powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07399775B2 |
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| 출처 데이터셋 | uspto-grants-2008_07 |
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| ORD ID | ord-a9ebf1a3b67445a0ace7f5f4238e70b6 |
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| 출처 메모 | uspto-grants-2008_07 |
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