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

HRID 1576439
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HRID 1576439 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-3039da87ec2f40d7ad7c06584cb263ca
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03980792

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