HCID 13058056, compound → 1,2-Dichloro-1-fluoro-2-(trifluoromethoxy)ethene

HRID 1440291Notes

Reaction equation

HRID 1440291 reaction equation
[Cl:1][C:2](Cl)([F:11])[C:3](Cl)([Cl:9])[O:4][C:5]([F:8])([F:7])[F:6].ClC(F)C(Cl)OC(F)(F)F>[Zn]>[Cl:1][C:2]([F:11])=[C:3]([Cl:9])[O:4][C:5]([F:8])([F:7])[F:6]

Participants

4

Conditions

Temperature
-75 °C

Procedure

In a 1 l three necked flask, equipped with magnetic stirrer, thermometer, dropping funnel, and connected through a Vigreux column and a condenser to a trap maintained at -75° C., 80.0 g of zinc powder, activated by washing with HCl 3N, 550 ml of DMF and 50 mg of KI were charged under nitrogen atmosphere. The internal temperature was brought to 80° C. and 102.0 g of 1,1,2,2-tetrachloro-1-fluoro-2-trifluoromethoxyethane (377mmoles), were added dropwise. During the addition, the temperature increased up to 90° C. When the addition was over, the reaction mixture was stirred for 1 additional hour at 90° C. In the cold trap 62.8 g (315 mmoles) of 1,2-dichloro-1-fluoro-2-trifluoromethoxyethane (cis/trans 50%/50%) condensed. The 1,2-dichloro-1-fluoro-2-trifluoromethoxyethene (trans+cis) yield was 83%.

Workup

  1. customconnected through a Vigreux column and a condenser to a trap
  2. washby washing with HCl 3N, 550 ml of DMF and 50 mg of KI
  3. additionwere charged under nitrogen atmosphere
  4. customwas brought to 80° C.
  5. additionDuring the addition
  6. temperaturethe temperature increased up to 90° C
  7. additionWhen the addition

Sources & evidence

ORD record
ord-c892faa71c3c44d0aa139666cd71a84a
Source dataset
uspto-grants-1996_03
Patent number
US05498682

Reaction notes

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