Chlorotrifluoroethylene → Perfluoropropionyl fluoride

HRID 6570

반응식

HRID 6570 반응식
C(C(C([O:10][C:11]([C:14]([C:17]([F:20])([F:19])[F:18])([F:16])[F:15])(F)[F:12])=O)(F)F)(F)(F)F.ClC(F)=C(F)F>[Ni].O>[C:17]([C:14]([C:11]([F:12])=[O:10])([F:16])[F:15])([F:20])([F:19])[F:18]

참가 물질

5

반응물 2

HCID 6594ChlorotrifluoroethyleneHCID 11381975Heptafluoropropyl pentafluoropropanoate

생성물 1

HCID 67912Perfluoropropionyl fluoride수율 90%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 962Water용매

반응 조건

온도
200 °C

실험 절차

CF3CF2COOCF2CF2CF3 (20 g) obtained in Example 5 and chlorotrifluoroethylene oligomer (120 g) were charged into a 200 ml autoclave made of nickel and equipped with a reflux condenser and heated to 200° C. The reflux condenser was cooled by circulating cooling water, and when the pressure became at least 0.1 MPa, the gas was purged while maintaining the pressure to recover a gaseous sample (15 g). By GC-MS, it was confirmed that CF3CF2COF was the main product. The GC yield was 90%.

후처리

  1. customequipped with a reflux condenser
  2. temperatureThe reflux condenser was cooled
  3. customthe gas was purged
  4. temperaturewhile maintaining the pressure
  5. customto recover a gaseous sample (15 g)

출처 및 근거

ORD 기록
ord-b089b4cdb71a4c93ac0c6b2f9f6f79ef
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07083705B2

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