2-Chloroethyl vinyl ether → [2-(Ethenyloxy)ethoxy]benzene

HRID 613451Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 613451
Cl[CH2:2][CH2:3][O:4][CH:5]=[CH2:6].[CH:7]1[CH:12]=[CH:11][C:10]([O-:13])=[CH:9][CH:8]=1.[Na+].C1(C2C(I=O)=C(S([O-])(=O)=O)C(C)=CC=2)C=CC=CC=1.[N-](S(C(F)(F)F)(=O)=O)S(C(F)(F)F)(=O)=O.[Na+]>ClCCl.Cl[Ti](Cl)(Cl)Cl.CC(CC)=O.C(O)(=O)C>[O:13]([CH2:6][CH2:5][O:4][CH:3]=[CH2:2])[C:10]1[CH:11]=[CH:12][CH:7]=[CH:8][CH:9]=1

Komponenten

9

Versuchsvorschrift

The compound phenoxyethylvinylether is prepared by reacting chloroethylvinylether with sodium phenate, followed by polymerization in dichloromethane initiated with TiCl4 at -10° C. By reacting 8.2 g of the polymer with 9.8 g of phenyliodosotoluene sulfonate in 40 mL of a mixture of an equal volume of acetic acid and dichloromethane. A polyiodonium is obtained which is precipitated with ether. The ionic exchange reaction is carried similarly to that of example 3 between 12 g of polymer and 7 g of sodium bis(trifluoromethanesulfonyl)imide. After precipitation and washing with water, there is obtained a sticky mass which is used in a 50% solution of methylethylketone.

Aufarbeitung

  1. customA polyiodonium is obtained which
  2. customis precipitated with ether
  3. customThe ionic exchange reaction
  4. customAfter precipitation
  5. washwashing with water
  6. customthere is obtained a sticky mass which

Quellen und Nachweise

ORD-Eintrag
ord-976dfdbd4e3545c19f9f87cbb4d04e15
Quelldatensatz
uspto-grants-1999_12
Patentnummer
US06008267

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