HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874243Erstellt: 25. Oktober 2026
Water → 3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene)
https://huagongshe.com/reaction/1874243
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Diethyl benzylphosphonate | HCID 14122 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Bis(3-(trifluoromethoxy)phenyl)methanone | HCID 59458637 | — |
| Katalysator | 15-Crown-5 | HCID 36336 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3,3'-(2-Phenylethene-1,1-diyl)bis((trifluoromethoxy)benzene) | HCID 59458604 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08304403B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-59f5cfe8f98c4ca6bc58b24e9fda190f |
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| Quellennotiz | uspto-grants-2012_11 |
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