Pinacol → 2-Allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane

HRID 493458

Reaktionsgleichung

Reaktionsgleichung von HRID 493458
[CH2:1]([Si:4]([Cl:7])(Cl)Cl)[CH:2]=[CH2:3].N12CCCN=C1CCCCC2.[OH:19][C:20]([C:23]([OH:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21]>C(Cl)Cl>[CH2:1]([Si:4]1([Cl:7])[O:26][C:23]([CH3:25])([CH3:24])[C:20]([CH3:22])([CH3:21])[O:19]1)[CH:2]=[CH2:3]

Komponenten

5

Versuchsvorschrift

To a cooled (0° C.) solution of allyltrichlorosilane (4.9 mL; 34 mmol) in CH2Cl2 (50 mL) was added 1,8-Diazabicyclo[5.4.0]undec-7-ene (13 mL; 84 mmol). A solution of pinacol (4.0 g; 34 mmol) in CH2Cl2 (50 mL) was then added slowly and the resultant solution was warmed to room temperature and stirred for 12 hours. The solution was concentrated and the residue was treated with diethylether (100 mL). The mixture was stirred for 1 hour during which time the formation of a precipitate was observed. The mixture was then filtered and the filtrate was concentrated. The residue was distilled under reduced pressure to give 5.2 g (72%) of 2-allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane as a clear, colorless liquid.

Aufarbeitung

  1. concentrationThe solution was concentrated
  2. additionthe residue was treated with diethylether (100 mL)
  3. stirringThe mixture was stirred for 1 hour during which time the formation of a precipitate
  4. filtrationThe mixture was then filtered
  5. concentrationthe filtrate was concentrated
  6. distillationThe residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-be5a5e9bd307417482280af77262364b
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07534905B2

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