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Chlorotrimethylsilane → 1,2-Ethanediamine, N,N'-dimethyl-N,N'-bis(trimethylsilyl)-

HRID 1283093
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1283093
[CH3:1][NH:2][CH2:3][CH2:4][NH:5][CH3:6].C(N(CC)CC)C.[CH3:14][Si:15]([CH3:18])([CH3:17])Cl>C1C=CC=CC=1>[CH3:1][N:2]([Si:15]([CH3:18])([CH3:17])[CH3:14])[CH2:3][CH2:4][N:5]([CH3:6])[Si:15]([CH3:18])([CH3:17])[CH3:14]
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Komponenten

5

Edukt 3

HCID 6397ChlorotrimethylsilaneHCID 8070N,N'-DimethylethylenediamineHCID 8471Triethylamine

Produkt 1

HCID 122268961,2-Ethanediamine, N,N'-dimethyl-N,N'-bis(trimethylsilyl)-

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel2×

Versuchsvorschrift

A mixture of 176 parts by weight of N,N'-dimethylethylenediamine, 1000 parts by volume of benzene and 552 parts by volume of triethylamine were stirred at room temperature and at the same time 434 parts by weight of trimethylchlorosilane, diluted with 500 parts by volume of benzene, were added dropwise over the course of 3 hours. The mixture was stirred for a further 3.5 hours and left to stand overnight, and the precipitate present was filtered off and washed with benzene. The combined filtrates were concentrated in a rotary evaporator and the residue was distilled in vacuo.

Aufarbeitung

  1. additionwere added dropwise over the course of 3 hours
  2. waitleft
  3. waitto stand overnight
  4. filtrationthe precipitate present was filtered off
  5. washwashed with benzene
  6. concentrationThe combined filtrates were concentrated in a rotary evaporator
  7. distillationthe residue was distilled in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d4f679d7c2ff44f0b4dbf1a155173380
Quelldatensatz
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US03974140

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