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HRID 1712786作成日:2026年10月27日

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

https://huagongshe.com/reaction/1712786

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl benzylphosphonateHCID 14122—
反応物Sodium hydrideHCID 24758—
反応物Bis(3-(trifluoromethoxy)phenyl)methanoneHCID 59458637—
触媒15-Crown-5HCID 36336—
溶媒TetrahydrofuranHCID 8028—
生成物3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)HCID 5945860453%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790770B2
出典データセットuspto-grants-2010_09
ORD IDord-f3bfa1f54127444a8fee4c4e1fa6e775
出典メモuspto-grants-2010_09