Trifluoroacetic acid → HCID 12269392, compound

HRID 1034368Notes

Reaction equation

HRID 1034368 reaction equation
FC(F)(F)C(O)=O.[Br:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH:15](O)[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C([SiH](CC)CC)C>>[Br:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

4

Reactant 3

HCID 6422Trifluoroacetic acidHCID 12052TriethylsilaneHCID 12715432HCID 12715432, compound

Product 1

HCID 12269392HCID 12269392, compoundYield 52%

Procedure

Trifluoroacetic acid (46 ml) was added in one portion to a stirred mixture of 1-(2-bromophenyl)-2-phenylethan-1-ol (16.51 g, prepared as described in Example 3) and triethylsilane (13.80 g). The resulting mixture was stirred at room temperature for about 22 hours, then the excess trifluoroacetic acid was removed under reduced pressure. The residue was dissolved in ether and washed successively with water, aqueous sodium bicarbonate (×3) and water (×2), then dried, concentrated under reduced pressure, and chromatographed using 10% dichloromethane in petrol as eluant to give 1-(2-bromophenyl)-2-phenylethane (8.02 g, 52%) as a colourless oil.

Workup

  1. customthe excess trifluoroacetic acid was removed under reduced pressure
  2. dissolutionThe residue was dissolved in ether
  3. washwashed successively with water, aqueous sodium bicarbonate (×3) and water (×2)
  4. customdried
  5. concentrationconcentrated under reduced pressure
  6. customchromatographed

Sources & evidence

ORD record
ord-a45cc60acc4a41189691a910db75fb18
Source dataset
uspto-grants-1994_05
Patent number
US05315025

Reaction notes

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