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Carbon Tetrachloride → N-(1-chloroethyl)-succinimide

HRID 127005
ノート
印刷プレビュー

反応式

HRID 127005 の反応式
[CH:1]([N:3]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]1=[O:9])=[CH2:2].C(Cl)(Cl)(Cl)[Cl:11]>>[Cl:11][CH:1]([N:3]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]1=[O:9])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 5943Carbon TetrachlorideHCID 219373N-Vinylsuccinimide

生成物 1

HCID 12439633N-(1-chloroethyl)-succinimide収率 59%

実験手順

N-vinylsuccinimide, 50.0 g (0.40 mole) is dissolved in 100 ml carbon tetrachloride, 5.20 g (0.020 mole) of stannic chloride is added and the mixture is stirred while saturating with hydrogen chloride gas for 6 hours at 20°-30° C. After 24 hours, the mixture is resaturated with hydrogen chloride gas for 1.5 hours. At the end of 48 hours, the solution is decanted and the gummy residue is washed with ten 100 ml portions of carbon tetrachloride. The combined extracts are slurried with 10 g of diatomaceous earth, filtered and the filtrate is concentrated under reduced pressure to approximately 400 ml. The N-(1-chloroethyl)-succinimide is filtered and dried at 20°-30° C. under reduced pressure to yield 38.4 g (59%) of white solid melting at 83.5°-84.5° C.

後処理

  1. concentrationwhile saturating with hydrogen chloride gas for 6 hours at 20°-30° C
  • waitthe mixture is resaturated with hydrogen chloride gas for 1.5 hours
  • customAt the end of 48 hours, the solution is decanted
  • washthe gummy residue is washed with ten 100 ml portions of carbon tetrachloride
  • filtrationfiltered
  • concentrationthe filtrate is concentrated under reduced pressure to approximately 400 ml
  • filtrationThe N-(1-chloroethyl)-succinimide is filtered
  • customdried at 20°-30° C. under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-c875a5ebe95b41bcb5b0af98809992c6
    出典データセット
    uspto-grants-1981_03
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04254273

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