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ChemicalBook CAS DataBase List Vinyl ether
109-93-3

Vinyl ether synthesis

9synthesis methods
Divinyl ether is prepared by the reaction of liquefied alkali hydroxide or sodium alkoxide on β,β_x0002_-dihalodiethyl ether or by pyrolysis of α,α_x0002_-dichlorodiethyl ether in the gas phase at 600 – 800 ?C in the presence of barium chloride catalyst .
-

Yield:-

Reaction Conditions:

in tert-butyl alcohol

Steps:

P.3.1 1.
1. Synthese von Divinylether In a100 mL two-neck flask equipped with a magnetic stirrer and a distillation bridge, 9.39 g (83.7 mmol) potassium tert-butylat in 40 mL wasserfreiem tert-Butanol are introduced and heated to 50 °C. By using a septum, 6.0 g (41.9 mmol) 2-chloroethyl ether is added dropwise to the mixture which is heated to 100 °C erhitzt. The reaction mixture becomes turbid. The Die distillation head is cooled with acetone/dry ice. GC/MS: m/z 70 (M+), 44 (C2H4O2+), 43 (C2H30+), 31 (CH30+), 27 (C2H3+). 1H-NMR(200 MHz, CDCl3): d 6.51-6.41 (dd, 2H, RO-CH=CH2), 4.62-4.54 (dd, 2H, RO-CH=CH2), 4.29-4.25 (dd, 2H, RO-CH=CH2) ppm.

References:

Dentsply DeTrey GmbH EP2316407, 2011, A1

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