2-Bromoethanol → 2,3-Benzofurandione, 2-[O-(2-hydroxyethyl)oxime] 3-(O-methyloxime)

HRID 1858135Notes

Reaction equation

HRID 1858135 reaction equation
[CH3:1][O:2][N:3]=[C:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]1=[N:13][OH:14].[H-].[Na+].Br[CH2:18][CH2:19][OH:20].C[O-].[Na+]>CN(C)C=O.O>[CH3:1][O:2][N:3]=[C:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]1=[N:13][O:14][CH2:18][CH2:19][OH:20]

Participants

7

Reactant 4

HCID 108982-Bromoethanol3×HCID 24758Sodium hydrideHCID 10942334Sodium Methoxide2×HCID 178502623HCID 178502623, compound

Product 1

HCID 543010792,3-Benzofurandione, 2-[O-(2-hydroxyethyl)oxime] 3-(O-methyloxime)Yield 40.9%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

4.49 g (0.0234 mol) of benzofuran-2,3-dione 3-(O-methyl-oxime) 2-oxime (VIII-1) are dissolved in 25 ml of dimethylformamide. 1 g (0.025 mol) of 60% strength sodium hydride is added to this solution which is then stirred at room temperature for one hour. 3.1 g (0.0248 mol) of 2-bromoethanol are added and the mixture is stirred at 25° C. for 12 hours. After the addition of 0.5 g of sodium methoxide and 1.22 g of 2-bromoethanol, the mixture is stirred at room temperature for 2 hours. A further 0.5 g of sodium methoxide and 1.22 g of 2-bromoethanol are added and the mixture is stirred for a further 2 hours at room temperature. The reaction mixture is poured into water and the resulting mixture is extracted with ethyl acetate and the organic phase is washed 3 times with 20 ml of 2 N aqueous sodium hydroxide solution. The solvent is distilled off under reduced pressure and the residue is chromatographed over silica gel using diethyl ether/petroleum ether (1:1). The eluent is distilled off under reduced pressure, affording 2.26 g (39.6% of theory) of benzofuran-2,3-dione 2-[O-(2-hydroxyethyl)-oxime] 3-(O-methyl-oxime) (II-1) which, according to HPLC, comprises 84.29% of stereoisomer A and 12.58% of stereoisomer B.

Workup

  1. stirringthe mixture is stirred at 25° C. for 12 hours
  2. stirringthe mixture is stirred at room temperature for 2 hours
  3. stirringthe mixture is stirred for a further 2 hours at room temperature
  4. extractionthe resulting mixture is extracted with ethyl acetate
  5. washthe organic phase is washed 3 times with 20 ml of 2 N aqueous sodium hydroxide solution
  6. distillationThe solvent is distilled off under reduced pressure
  7. customthe residue is chromatographed over silica gel
  8. distillationThe eluent is distilled off under reduced pressure

Sources & evidence

ORD record
ord-f4e0fbcb85fe4498b9acc9c2b97eb79f
Source dataset
uspto-grants-2000_11
Patent number
US06150521

Reaction notes

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