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HRID 1712786Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1712786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiethyl benzylphosphonateHCID 14122—
EduktSodium hydrideHCID 24758—
EduktBis(3-(trifluoromethoxy)phenyl)methanoneHCID 59458637—
Katalysator15-Crown-5HCID 36336—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)HCID 5945860453%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790770B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-f3bfa1f54127444a8fee4c4e1fa6e775
Quellennotizuspto-grants-2010_09