Potassium Hydroxide → 3-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctyloxymethyl)-3-methyloxetane
Reaktionsgleichung
Br[CH2:2][C:3]1([CH3:7])[CH2:6][O:5][CH2:4]1.[F:8][C:9]([F:31])([C:12]([F:30])([F:29])[C:13]([F:28])([F:27])[C:14]([F:26])([F:25])[C:15]([F:24])([F:23])[C:16]([F:22])([F:21])[C:17]([F:20])([F:19])[F:18])[CH2:10][OH:11].[OH-].[K+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[F:8][C:9]([F:31])([C:12]([F:29])([F:30])[C:13]([F:27])([F:28])[C:14]([F:25])([F:26])[C:15]([F:23])([F:24])[C:16]([F:22])([F:21])[C:17]([F:20])([F:19])[F:18])[CH2:10][O:11][CH2:2][C:3]1([CH3:7])[CH2:6][O:5][CH2:4]1Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
In a manner similar to the that of Example B14, a mixture of 3-bromomethyl-3-methyloxetane (468 g, 2.84 mol), 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctan-1-ol (1032 g, 2.58 mol), tetrabutylammonium bromide (41.5 g), potassium hydroxide (208 g, 3.23 mol), and water (1680 ml) was heated under reflux for 3 hours. GLC analysis revealed complete consumption of starting materials. The reaction mixture was diluted with water, worked-up in the usual manner, and distilled under reduced pressure to give 1,085 g of 15-FOX, representing an overall yield of 87%; bp 82° C./0.1 mm-Hg. The distilled material was >99% pure as indicated by GLC and was used in subsequent polymerization reactions.
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 3 hours
- customconsumption of starting materials
- additionThe reaction mixture was diluted with water
- distillationdistilled under reduced pressure
- customto give 1,085 g of 15-FOX,
- customwas used in subsequent polymerization reactions
Quellen und Nachweise
- ORD-Eintrag
- ord-a299b5ee5b6f418d8013c541bce79efe
- Quelldatensatz
- uspto-grants-2002_04
- Patentnummer
- US06380351B1
Notizen zur Reaktion
Wird geladen…