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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Chlorotrimethylsilane → 2,5-Pyrrolidinedione, 1-(trimethylsilyl)-

HRID 436029
ノート
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反応式

HRID 436029 の反応式
[CH3:1][Si:2]([CH3:5])([CH3:4])Cl.[C:6]1(=[O:12])[NH:10][C:9](=[O:11])[CH2:8][CH2:7]1.C(N(CC)CC)C>C1(C)C=CC=CC=1>[CH3:1][Si:2]([CH3:5])([CH3:4])[N:10]1[C:6](=[O:12])[CH2:7][CH2:8][C:9]1=[O:11]
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 8471TriethylamineHCID 11439Succinimide

生成物 1

HCID 116654792,5-Pyrrolidinedione, 1-(trimethylsilyl)-収率 85%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

780 ml (6.1 moles) of trimethylchlorosilane were added with vigorous stirring over 2 hours to a mixture of 400 g (4 moles) of succinimide, 900 ml (6.5 moles) of triethylamine and 2700 ml of toluene and the mixture was refluxed with stirring for one hour and was then cooled to room temperature. The mixture was filtered and the filter was washed with one liter of toluene and one liter of petroleum ether (b.p = 40°-60° C). The combined filtrate and washings were concentrated to 700 ml and then distilled at reduced pressure to 573 g (3.4 moles -- 84% yield) of N-trimethylsilyl succinimide with a boiling point of 62° C at 0.33 mm Hg.

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. temperaturethe mixture was refluxed
  2. filtrationThe mixture was filtered
  3. washthe filter was washed with one liter of toluene and one liter of petroleum ether (b.p = 40°-60° C)
  4. concentrationThe combined filtrate and washings were concentrated to 700 ml

出典と根拠

ORDレコード
ord-2622620a1dca42ad80560f979461f04e
出典データセット
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04007202

反応ノート

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