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HCID 54187688, 화합물 → 4-Chlorophthalic anhydride

HRID 1111180
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HRID 1111180 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 54187688HCID 54187688, 화합물

생성물 1

HCID 670444-Chlorophthalic anhydride수율 67%

시약·촉매·용매 1

HCID 131,2,4-Trichlorobenzene용매

반응 조건

온도
230 °C

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-556810063feb4b12b18147101638a31f
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04978760

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