Sulfate Ion → 1,2,3,4-Tetrafluorobenzene

HRID 622255

반응식

HRID 622255 반응식
[F:1][C:2]1[C:10]([F:11])=[C:9]([F:12])[C:8]([F:13])=[C:4](C(O)=O)[C:3]=1C(O)=O.S([O-])([O-])(=O)=[O:18].[OH-].[Na+]>O>[F:1][C:2]1[CH:3]=[CH:4][C:8]([F:13])=[C:9]([F:12])[C:10]=1[F:11].[F:1][C:2]1[CH:3]=[CH:4][C:8]([OH:18])=[C:9]([F:12])[C:10]=1[F:11]

참가 물질

6

반응물 3

HCID 1117Sulfate IonHCID 14798Sodium HydroxideHCID 695443,4,5,6-Tetrafluorophthalic acid

생성물 2

HCID 110841,2,3,4-TetrafluorobenzeneHCID 1231742,3,4-Trifluorophenol

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
200 °C

실험 절차

In an autoclave having an inner volume of 100 ml, 3.0 g (0.0126 mole) of 3,4,5,6-tetrafluorophthalic acid containing no sulfate ion, 0.5 g (0.0125 mole) of sodium hydroxide, and 50 g of water were placed and heated for reaction at 200° C. for 25 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and extracted with 150 ml of diisopropyl ether. By analyzing this extract by gas chromatography using a 2 m column packed with SE52 and kept at 50° C., the reaction was found to have produced 2.9 mole % of 1,2,3,4-tetrafluorobenzene, 89.1 mole % of trifluorophenol, and substantially no 2,3,4,5-tetrafluorobenzoic acid based on the 3,4,5,6-tetrafluorophthalic acid used as the starting material [pH 2.75 at 25° C. at the time of charging].

후처리

  1. customAfter completion of the reaction
  2. temperaturethe reaction mixture was cooled to room temperature
  3. extractionextracted with 150 ml of diisopropyl ether
  4. extractionthis extract by gas chromatography
  5. customkept at 50° C.

출처 및 근거

ORD 기록
ord-cd5760b79d004bedb9f906022f11db42
출처 데이터셋
uspto-grants-1988_09
특허 번호
US04769492

연결된 노트

불러오는 중…