Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 985042생성일: 2026년 10월 25일
Bis(trifluoroacetoxy)iodobenzene → 4-[[3-Methyl-4-(4-trifluoromethylbenzyloxy)phenyl]sulfanyl]-2-propylphenoxy-acetic acid ethyl ester
https://huagongshe.com/reaction/985042
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bis(trifluoroacetoxy)iodobenzene | HCID 102317 | — |
| 반응물 | 2-[4-(Trifluoromethyl)benzyloxy]toluene | HCID 11219321 | — |
| 반응물 | 4-Mercapto-2-propylphenoxy-acetic acid ethyl ester | HCID 20768111 | — |
| 용매 | 1,1,1,3,3,3-Hexafluoro-2-propanol | HCID 13529 | — |
| 생성물 | 4-[[3-Methyl-4-(4-trifluoromethylbenzyloxy)phenyl]sulfanyl]-2-propylphenoxy-acetic acid ethyl ester | HCID 59129124 | 59.9% |
반응 단계
Compound 4.4 (5.0 g, 19.66 mmol) was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (30 mL) under argon atmosphere. To the solution was added compound 4.1 (5.23 g, 19.66 mmol) and [bis(trifluoroacetoxy)iodo]benzene (10.14 g, 23.59 mmol) slowly, while maintaining the reaction temperature between 10° C. and 17° C. After stirring for 15 min, the reaction mixture was concentrated in vacuo to give a residue which was purified using silica gel column chromatography (hexane/EtOAc=20/1) to give 4.5 (6.11 g). 1H NMR (400 MHz) (CDCl3) δ 7.64 (2H, d, J=8.2 Hz); 7.54 (2H, d, J=8.1 Hz); 7.20-7.06 (4H, m); 6.76 (1H, d, J=8.4 Hz); 6.62 (1H, d, J=8.4 Hz); 5.11 (2H, s); 4.60 (2H, s); 4.25 (2H, q, J=7.1 Hz); 2.63-2.56 (2H, m); 2.24 (3H, s); 1.67-1.55 (2H, m); 1.28 (3H, t, J=7.1 Hz); 0.92 (3H, t, J=7.4 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06869975B2 |
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| 출처 데이터셋 | uspto-grants-2005_03 |
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| ORD ID | ord-38d2925e64434a719c7daf17bfbbfdea |
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| 출처 메모 | uspto-grants-2005_03 |
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