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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1712786생성일: 2026년 10월 26일

Water → 3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)

https://huagongshe.com/reaction/1712786

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diethyl benzylphosphonateHCID 14122—
반응물Sodium hydrideHCID 24758—
반응물Bis(3-(trifluoromethoxy)phenyl)methanoneHCID 59458637—
촉매15-Crown-5HCID 36336—
용매TetrahydrofuranHCID 8028—
생성물3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)HCID 5945860453%

반응 단계

To a suspension of NaH (60% in oil, 0.24 g, 6 mmol) in dry THF (25 mL) under nitrogen was added 15-crown-5 (0.06 g). The suspension was cooled in an ice bath. Bis(3-(trifluoromethoxy)phenyl)methanone (2.10 g, 6 mmol) and diethyl benzylphosphonate (1.37 g, 6 mmol) were dissolved in THF (12 mL) and added to the suspension. The reaction mixture was stirred at ice bath temperature for 15 min, allowed to warm to rt and stirred overnight. The reaction mixture was poured into water and extracted with ether (2×). The combined ether layers were washed with 10% NaHSO3, sat. NaCl, dried over K2CO3, filtered and purified by ISCO using a gradient of 0-4% EtOAc/hexanes as eluent to give 3,3′-(2-phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene) as a colorless oil (1.34 g, 53% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.33 (m, 2H), 7.2-7.1 (m, 8H), 7.04 (s, 1H), 7.0-6.97 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790770B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-f3bfa1f54127444a8fee4c4e1fa6e775
출처 메모uspto-grants-2010_09