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m-Chloroperbenzoic acid → HCID 86735257、化合物

HRID 461405
ノート
印刷プレビュー

反応式

HRID 461405 の反応式
[Cl:1][CH:2]=[CH:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.ClC1C=CC=C(C(OO)=[O:19])C=1>C(Cl)(Cl)Cl>[Cl:1][CH:2]=[CH:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]2[O:19][CH:7]2[CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 138711(3-Chloroallyl)benzene

生成物 1

HCID 86735257HCID 86735257、化合物収率 55.7%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

24.6 g of p-chloroallylbenzene was dissolved in 100 ml of chloroform and to the mixture was added dropwise, while maintaining the temperature at 0° - 5° C, 34.5 g of m-chloroperbenzoic acid dissolved in 1l of chloroform. The resulting mixture was allowed to stand at the same temperature for 72 hours. After the separated m-chlorobenzoic acid was filtered off, the filtrate was washed with 10% sodium hydroxide solution, then with water and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain the residue, which was distilled under reduced pressure to give 15.1 g (yield 55.7%) of p-chloroallylbenzene oxide having a boiling point of 96° C/2.5 mmHg.

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. additionwas added dropwise
  2. temperaturewhile maintaining the temperature at 0° - 5° C
  3. filtrationAfter the separated m-chlorobenzoic acid was filtered off
  4. washthe filtrate was washed with 10% sodium hydroxide solution
  5. dry with materialwith water and dried over anhydrous sodium sulfate
  6. customThe solvent was evaporated
  7. customto obtain the residue, which
  8. distillationwas distilled under reduced pressure

出典と根拠

ORDレコード
ord-e79e175c486d424c85cbe67ac99f86e3
出典データセット
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04062862

反応ノート

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