Water → HCID 21529354, compound

HRID 1658415Notes

Reaction equation

HRID 1658415 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

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 The organic phase was withdrawn, washed with saturated aqueous sodium chloride, dried (MgSO4), and distilled to give 3.9 g of 3-methoxy-2,4,4-trifluorocyclobut-2-en-1-one (3): bp 58°(10 mm).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

  1. temperatureabove was chilled to -78°
  2. dissolutiondissolved
  3. customThe organic phase was withdrawn
  4. washwashed with saturated aqueous sodium chloride
  5. dry with materialdried (MgSO4)
  6. distillationdistilled

Sources & evidence

ORD record
ord-03c55adabc214b2a89310850781b7119
Source dataset
uspto-grants-1976_06
Patent number
US03963767

Reaction notes

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