Acetic Acid → 4-(6-Hydroxy-2,2,3,3,4,4,5,5-octafluorohexyloxy)tetrafluoronitrobenzene

HRID 1638114Notes

Reaction equation

HRID 1638114 reaction equation
[F:1][C:2]([F:16])([C:5]([F:15])([F:14])[C:6]([F:13])([F:12])[C:7]([F:11])([F:10])[CH2:8][OH:9])[CH2:3][OH:4].[F:17][C:18]1[C:23]([N+:24]([O-:26])=[O:25])=[C:22]([F:27])[C:21]([F:28])=[C:20](F)[C:19]=1[F:30].C(N(CC)CC)C.C(O)(=O)C>CN1C(=O)CCC1.O>[OH:9][CH2:8][C:7]([F:10])([F:11])[C:6]([F:13])([F:12])[C:5]([F:14])([F:15])[C:2]([F:16])([F:1])[CH2:3][O:4][C:20]1[C:19]([F:30])=[C:18]([F:17])[C:23]([N+:24]([O-:26])=[O:25])=[C:22]([F:27])[C:21]=1[F:28]

Participants

7

Procedure

A mixture of 2,2,3,3,4,4,5,5-octafluoro-1,6-hexanediol (7.86 g) was treated with pentafluoronitrobenzene (2.13 g) and triethylamine (1.39 mL,) in NMP (15 mL) at room temperature for 1 hr. The mixture was diluted with water, acidified with acetic acid, and extracted with ethyl ether. The extract was washed with water and brine; dried (MgSO4) and concentrated. Excess diol was removed by distillation and the residual oil purified by chromatography to give 4-(6-hydroxy-2,2,3,3,4,4,5,5-octafluorohexyloxy)tetrafluoronitrobenzene (3.06 g).

Workup

  1. extractionextracted with ethyl ether
  2. washThe extract was washed with water and brine
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. customExcess diol was removed by distillation
  6. customthe residual oil purified by chromatography

Sources & evidence

ORD record
ord-a59dabe2a05844e688770e899ebcf4ee
Source dataset
uspto-grants-2000_03
Patent number
US06043337

Reaction notes

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