Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Cyanophenol | HCID 13019 | — |
| Edukt | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 14008159 | HCID 14008159 | 65,1% |
Reaktionsschritte
10 g (0.092 mol) of α-fluoroacryloyl chloride (obtained in accordance with example 1c) were added dropwise, at a temperature of 5° C., with stirring and in the course of 20 minutes, to a solution of 10.7 g (0.09 mol) of 4-cyanophenol and 9.1 g (0.09 mol) of triethylamine in 150 ml of anhydrous methylene dichloride, and the reaction mixture was then stirred for a further 30 minutes at the same temperature. The solid formed was filtered off and washed with 20 ml of anhydrous methylene dichloride. After 0.005 g of hydroquinone monomethyl ether had been added, the volatile constituents in the mixture of filtrate and wash solution were removed by distillation, and the residue was recrystallized from boiling n-hexane. 11.2 g (65% of theory) of 4-cyanophenyl α-fluoroacrylate were obtained, melting point 78° to 79° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05266668 |
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| Quelldatensatz | uspto-grants-1993_11 |
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| ORD ID | ord-48cedf718b7546a68e7ab87cdf1effe4 |
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| Quellennotiz | uspto-grants-1993_11 |
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