Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9344생성일: 2026년 10월 23일
Triphenylphosphine → {4-[3,3-Bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester
https://huagongshe.com/ko/reaction/9344
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 반응물 | 3,3-Bis-(4-pyridin-3-yl-phenyl)-prop-2-en-1-ol | HCID 21986819 | — |
| 반응물 | Ethyl [4-sulfanyl-2-(trifluoromethyl)phenoxy]acetate | HCID 59516001 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | {4-[3,3-Bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester | HCID 69620630 | — |
반응 단계
Triphenylphosphine (138 mg, 0.68 mmol) and ADDP (173 mg, 0.68 mmol) were added to a solution of 3,3-bis-(4-pyridin-3-yl-phenyl)-prop-2-en-1-ol (100 mg, 0.27 mmol) in THF (5 ml) at 0° C. The reaction mixture was stirred for 5 min under nitrogen atmosphere. (4-Mercapto-2-trifluoromethyl-phenoxy)-acetic acid ethyl ester (prepared analogous to procedure in BioOrg. Med. Chem. Lett. 2003, 13, 1517) (92 mg, 0.32 mmol) was slowly added to the reaction mixture and the reaction was stirred for further 2 h at 0° C. The reaction mixture was evaporated and the residue was triturated with ether (2×15 ml). The filtered ether phases were evaporated and purified by column chromatography (eluent: ethyl acetate) to give {4-[3,3-bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester in 100 mg (60%) yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091245B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-c5ebe0b0aed846cc89d4466e7663f9a1 |
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| 출처 메모 | uspto-grants-2006_08 |
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