Water → HCID 21529354, compound
Reaction equation
F[Sb-](F)(F)(F)(F)F.[CH3:8][O:9][CH2+:10]1[C:13]([F:15])([F:14])[C:12](F)=[C:11]1[F:17].[OH2:18]>C(Cl)Cl>[CH3:8][O:9][C:10]1[C:13]([F:15])([F:14])[C:12](=[O:18])[C:11]=1[F:17]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The antimonate (2) solution in SO2 prepared substantially as above was chilled to -78° and added cautiously to 200 ml of vigorously stirred iced water. After warming to room temperature and stirring until all the solid dissolved, 25 ml of methylene chloride was added. The organic phase was withdrawn, washed with saturated aqueous sodium chloride, dried (MgSO4), and distilled to give 3.9 g of 3-methoxy-2,4,4-trifluorocyclobut-2-en-1-one (3): bp 58°(10 mm). ##SPC5##
Workup
- temperatureabove was chilled to -78°
- dissolutiondissolved
- customThe organic phase was withdrawn
- washwashed with saturated aqueous sodium chloride
- dry with materialdried (MgSO4)
- distillationdistilled
Sources & evidence
- ORD record
- ord-03c55adabc214b2a89310850781b7119
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03963767
Reaction notes
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