Toluene → 4-(2-Thienylmethyl)-2,2,6,6-tetra-methyl-1-oxa-4-aza-2,6-disilacyclohexane

HRID 27876

Reaktionsgleichung

Reaktionsgleichung von HRID 27876
[C:1]1([CH2:6][NH2:7])[S:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C.Cl[CH2:16][Si:17]([CH3:25])([CH3:24])[O:18][Si:19]([CH2:22]Cl)([CH3:21])[CH3:20].C1(C)C=CC=CC=1>O>[S:5]1[CH:4]=[CH:3][CH:2]=[C:1]1[CH2:6][N:7]1[CH2:20][Si:19]([CH3:22])([CH3:21])[O:18][Si:17]([CH3:25])([CH3:24])[CH2:16]1

Komponenten

6

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a solution containing 22.6 g. (0.2 mole) of 2-thenylamine, 44.4 g. (0.44 mole) of triethylamine and 50.0 g. of acetonitrile dried over molecular sieves there is added 46.2 g. (0.2 mole) of 1,3-bis-chloromethyl-1,1,3,3-tetramethyl-disiloxane. The resulting homogenized solution is allowed to stand for 3 days and then heated in a bath at 90° C. for 36 hours. After cooling the mixture is then equiliberated between toluene and water, the organic phase is then washed with two more portions of water and concentrated to give 61.5 g. of a crude oil. Vacuum distillation through a Vigreux column gives 4-(2-thienylmethyl)-2,2,6,6-tetra-methyl-1-oxa-4-aza-2,6-disilacyclohexane; b.p. 78° to 80° C. at 0.1 to 0.11 mm.

Aufarbeitung

  1. additionTo a solution containing 22.6 g
  2. dry with materialof acetonitrile dried over molecular sieves there
  3. additionis added 46.2 g
  4. temperatureAfter cooling the mixture
  5. washthe organic phase is then washed with two more portions of water
  6. concentrationconcentrated
  7. customto give 61.5 g
  8. distillationVacuum distillation through a Vigreux column

Quellen und Nachweise

ORD-Eintrag
ord-daa0191ef4ad4921942a85e01f0b9bb3
Quelldatensatz
uspto-grants-1980_09
Patentnummer
US04224317

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