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Dimethylacetamide → 2,3,5,6-Tetrafluorobenzoic Acid

HRID 482145
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인쇄 미리보기

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HRID 482145 반응식
CN(C)C(=O)C.[F:7][C:8]1[C:16]([F:17])=[C:15](C(O)=O)[C:14]([F:21])=[C:13]([F:22])[C:9]=1[C:10]([OH:12])=[O:11]>O>[F:7][C:8]1[C:16]([F:17])=[CH:15][C:14]([F:21])=[C:13]([F:22])[C:9]=1[C:10]([OH:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31374DimethylacetamideHCID 695492,3,5,6-Tetrafluoroterephthalic acid

생성물 1

HCID 5675332,3,5,6-Tetrafluorobenzoic Acid수율 98%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
20 °C

실험 절차

N,N-Dimethylacetamide (14.0 parts) and 2,3,5,6-tetrafluoroterephthalic acid (2.91 parts) was heated at 70° C. for 4 hours before cooling to 20° C. adding water (7 parts) and cooling to 5° C. The precipitated solid was collected by filtration and washed with cold water and dried, the aqueous filtrates were evaporated under vacuum and the resultant solids combined to give 2,3,5,6-tetrafluorobenzoic acid (98%). 1,2,4,5-tetrafluorobenzene (2%) was also formed.

후처리

  1. temperaturecooling to 5° C
  2. filtrationThe precipitated solid was collected by filtration
  3. washwashed with cold water
  4. customdried
  5. customthe aqueous filtrates were evaporated under vacuum

출처 및 근거

ORD 기록
ord-c0a4bb5b3740452caefe96c7cf33b70b
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05792887

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