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

HRID 1576439
ノート
印刷プレビュー

反応式

HRID 1576439 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-3039da87ec2f40d7ad7c06584cb263ca
出典データセット
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03980792

反応ノート

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