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HCID 54187688、化合物 → 4-Chlorophthalic anhydride

HRID 1111180
ノート
印刷プレビュー

反応式

HRID 1111180 の反応式
[Cl:1][CH:2]1[CH:12]=[CH:11][CH:5]2[C:6]([O:8][C:9](=[O:10])[CH:4]2[CH2:3]1)=[O:7]>ClC1C=CC(Cl)=CC=1Cl>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[O:8][C:6](=[O:7])[C:5]2=[CH:11][CH:12]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 54187688HCID 54187688、化合物

生成物 1

HCID 670444-Chlorophthalic anhydride収率 67%

試薬・触媒・溶媒 1

HCID 131,2,4-Trichlorobenzene溶媒

反応条件

温度
230 °C

実験手順

Into a 3 necked round bottom flask is placed 49.47 grams of 4-chlorotetrahydrophthalic anhydride, 20.26 g activated carbon (NORIT CA-1) and 200 ml of 1,2,4-trichlorobenzene. The flask is fitted with an air inlet tube, a stirrer, and an addition funnel-condenser to collect water and allow the reflux to return to the flask. The flask was heated and raised to 230° C. with a constant flow of air. The reaction was conducted for eight hours. The carbon was removed by filtration and washed. The contents was concentrated under vacuum and analysis confirmed a yield of 67% 4-chlorophthalic anhydride and 4% of unreacted starting material.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. customThe flask is fitted with an air inlet tube, a stirrer, and an addition funnel-condenser
  2. customto collect water
  3. temperaturereflux
  4. temperatureThe flask was heated
  5. customThe carbon was removed by filtration
  6. washwashed
  7. concentrationThe contents was concentrated under vacuum and analysis

出典と根拠

ORDレコード
ord-556810063feb4b12b18147101638a31f
出典データセット
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04978760

反応ノート

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