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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712786Generated: October 26, 2026

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

https://huagongshe.com/reaction/1712786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl benzylphosphonateHCID 14122—
ReactantSodium hydrideHCID 24758—
ReactantBis(3-(trifluoromethoxy)phenyl)methanoneHCID 59458637—
Catalyst15-Crown-5HCID 36336—
SolventTetrahydrofuranHCID 8028—
Product3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)HCID 5945860453%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790770B2
Source datasetuspto-grants-2010_09
ORD IDord-f3bfa1f54127444a8fee4c4e1fa6e775
Source noteuspto-grants-2010_09