Water → HCID 20348777, compound

HRID 1701171Notes

Reaction equation

HRID 1701171 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][C:11]([CH:14]([S:16]([CH2:18][C:19]([OH:21])=[O:20])=[O:17])[CH3:15])=[CH:10][CH:9]=1.S(=O)(=O)(O)[OH:23].O.[Mn]([O-])(=O)(=O)=O.[K+]>CC(C)=O>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][C:11]([CH:14]([S:16]([CH2:18][C:19]([OH:21])=[O:20])(=[O:23])=[O:17])[CH3:15])=[CH:10][CH:9]=1

Participants

6

Procedure

170 gm (0.556 mol) of a diastereoisomeric mixture of [1-(2'-fluoro-4-biphenylyl)-ethylsulfinyl]-acetic acid were dissolved in 1.7 liters of acetone, and a solution of 19.9 gm (0.195 mol) of concentrated sulfuric acid inf 70 ml of water was added. While stirring, 67.2 gm (0.425 mol) of potassium permanganate were added in small portions, and the temperature was maintained at 20°-25° C. The mixture was stirred for 1 hour, the manganese dioxide was suction-filtered off, the filter cake was washed with acetone, and the filtrate was evaporated in vacuo. The residue was diluted with 4 liters of glacial acetic acid, and the precipitated crystalline reaction product was suction-filtered off, washed, dried and recrystallized from toluene. Yield: 158.2 gm (88.5% of theory); m.p. 144°-146° C.

Workup

  1. temperaturethe temperature was maintained at 20°-25° C
  2. stirringThe mixture was stirred for 1 hour
  3. filtrationthe manganese dioxide was suction-filtered off
  4. washthe filter cake was washed with acetone
  5. customthe filtrate was evaporated in vacuo
  6. additionThe residue was diluted with 4 liters of glacial acetic acid
  7. filtrationthe precipitated crystalline reaction product was suction-filtered off
  8. washwashed
  9. customdried
  10. customrecrystallized from toluene

Sources & evidence

ORD record
ord-00f9956aa7974a279407838172deb219
Source dataset
uspto-grants-1980_03
Patent number
US04191776

Reaction notes

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