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

HRID 493458

反応式

HRID 493458 の反応式
[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]

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-be5a5e9bd307417482280af77262364b
出典データセット
uspto-grants-2009_05
特許番号
US07534905B2

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