Diethyl Ether → MAU 2,2,3,3-tetrafluoropropyl methacrylate

HRID 405656

Reaktionsgleichung

[C:1]([NH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:20]([O:25][CH2:26][C:27]([F:32])([F:31])[CH:28]([F:30])[F:29])(=[O:24])[C:21]([CH3:23])=[CH2:22].C(OCC)C>CO.N(C(C)(C)C#N)=NC(C)(C)C#N>[C:1]([NH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:20]([O:25][CH2:26][C:27]([F:31])([F:32])[CH:28]([F:29])[F:30])(=[O:24])[C:21]([CH3:23])=[CH2:22]

Komponenten

Reaktionsbedingungen

Temperatur: 60 °C

Versuchsvorschrift

In 59.69 g of methanol were dissolved 18.47 g (68.60 mmol) of 11-methacrylamidoundecanoic acid (MAU), 1.53 g (7.62 mmol) of 2,2,3,3-tetrafluoropropyl methacrylate (Tokyo Chemical industry Co.), and 0.31 g (1.89 mmol) of azobisisobutyronitrile (Nacalai Tesque, Inc.). The solution was deaerated by bubbling nitrogen for 60 minutes. The container was covered with a septum, and the polymerization was conducted by heating at 60° C. for 20 hours. After the completion of the polymerization reaction, the reaction solution was dropwise added into a large excess of diethyl ether, and the resulting precipitate was collected by filtration under suction. After drying under reduced pressure, 16.15 g of random MAU/2,2,3,3-tetrafluoropropyl methacrylate copolymer (90/10) was obtained (yield: 80.8%). The weight average molecular weight was 220000.

Aufarbeitung

customby bubbling nitrogen for 60 minutes
customAfter the completion of the polymerization reaction
filtrationthe resulting precipitate was collected by filtration under suction
customAfter drying under reduced pressure

Quellen und Nachweise

ORD-Eintrag: ord-9dd40ec1c474402fb4e16fb3cddbbf5d
Quelldatensatz: uspto-grants-2014_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08753686B2

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