Ethylene Glycol → HCID 13691086, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:20])([F:19])[C:9]([C:12]2[CH:17]=[CH:16][C:15](F)=[CH:14][CH:13]=2)([F:11])[F:10])=[CH:4][CH:3]=1.[CH2:21]([OH:24])[CH2:22][OH:23]>>[OH:23][CH2:22][CH2:21][O:24][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:20])([F:19])[C:9]([C:12]2[CH:17]=[CH:16][C:15]([O:23][CH2:22][CH2:21][OH:24])=[CH:14][CH:13]=2)([F:11])[F:10])=[CH:4][CH:3]=1Participants
3
Conditions
- Temperature
- 150 °C
Procedure
700 ml of ethylene glycol and 65 g of 1,2-bis(4-fluorophenyl)-1,1,2,2-tetrafluoroethane* are heated to 110° C. in a stirred flask. 57 g of potassium tert.-butylate are added in portions and the mixture is then stirred at 150° C. for 7 hours. The mixture is cooled, poured onto 4 liters of ice-water and mixed thoroughly with a homogenizer (Ultraturax). The crystals which have precipitated are filtered-off with suction, stirred again with 2 liters of water filtered-off with suction again, dried and recrystallized from toluene.
Workup
- temperatureThe mixture is cooled
- additionmixed thoroughly with a homogenizer (Ultraturax)
- customThe crystals which have precipitated
- stirringstirred again with 2 liters of water filtered-off with suction again
- customdried
- customrecrystallized from toluene
Sources & evidence
- ORD record
- ord-ad29db34c37e40fb8989ea8c1e305f14
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04665217
Reaction notes
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