Sodium Hydroxide → HCID 10454998, compound

HRID 618766Notes

Reaction equation

HRID 618766 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][S:14][C:15]2[CH:27]=[C:26]([F:28])[C:18]([O:19][CH2:20][C:21](OCC)=[O:22])=[C:17]([F:29])[CH:16]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+].S([O-])([O-])(=O)=O.[Na+].[Na+]>C(OCC)(=O)C.O1CCCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][S:14][C:15]2[CH:16]=[C:17]([F:29])[C:18]([O:19][CH2:20][CH2:21][OH:22])=[C:26]([F:28])[CH:27]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1

Participants

7

Procedure

To a mixture of ethyl 4-[2-(4-chlorophenylsulfonylamino)ethylthio]-2,6-difluorophenoxyacetate (0.46 g) and tetrahydrofuran (30 ml) was added under ice cooling lithium aluminum hydride (38 mg), and the mixture was stirred at room temperature for an hour. To the reaction mixture was added successively 10% aqueous sodium hydroxide solution (0.2 ml), ethyl acetate (30 ml) and anhydrous sodium sulfate (1 g), and the insolubles were removed by filtration. After evaporation of the filtrate under reduced pressure, the residue was chromatographed on silica gel column (eluent; ethyl acetate:hexane=1:1), and the desired fractions were collected and recrystallized from ethyl ether/isopropyl ether mixture to give 2-{4-[2-(4-chlorophenylsulfonylamino)ethylthio]-2,6-difluorophenoxy}ethanol (Compound No. 129).

Workup

  1. additionwas added under ice
  2. customthe insolubles were removed by filtration
  3. customAfter evaporation of the filtrate under reduced pressure
  4. customthe residue was chromatographed on silica gel column (eluent; ethyl acetate:hexane=1:1)
  5. customthe desired fractions were collected
  6. customrecrystallized from ethyl ether/isopropyl ether mixture

Sources & evidence

ORD record
ord-f8e67e4b6b1645ed94bd3a9e99085865
Source dataset
uspto-grants-1999_09
Patent number
US05955505

Reaction notes

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