Chlorotrifluoroethylene → Perfluoropropionyl fluoride

HRID 6570

反応式

HRID 6570 の反応式
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]

参加物

5

反応物 2

HCID 6594ChlorotrifluoroethyleneHCID 11381975Heptafluoropropyl pentafluoropropanoate

生成物 1

HCID 67912Perfluoropropionyl fluoride収率 90%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 962Water溶媒

反応条件

温度
200 °C

実験手順

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%.

後処理

  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)

出典と根拠

ORDレコード
ord-b089b4cdb71a4c93ac0c6b2f9f6f79ef
出典データセット
uspto-grants-2006_08
特許番号
US07083705B2

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