Hydrogen Peroxide → HCID 22730343, compound

HRID 2356132Notes

Reaction equation

HRID 2356132 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH:9]=[CH2:10])[CH:6]=[CH:5][C:4]=1[C:11]1[CH:16]=[CH:15][C:14]([C:17]([O:19][CH3:20])=[O:18])=[CH:13][CH:12]=1.B.C(=O)([O-])[O-:23].[Na+].[Na+].OO>C1COCC1.C(OCC)(=O)C>[OH:23][CH2:10][CH2:9][C:7]1[CH:6]=[CH:5][C:4]([C:11]2[CH:12]=[CH:13][C:14]([C:17]([O:19][CH3:20])=[O:18])=[CH:15][CH:16]=2)=[C:3]([O:2][CH3:1])[CH:8]=1

Participants

7

Reactant 4

HCID 784Hydrogen PeroxideHCID 6331BoraneHCID 10340Sodium CarbonateHCID 22730842HCID 22730842, compound

Product 1

HCID 22730343HCID 22730343, compound

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent2×HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
60 °C

Procedure

A solution of Example 445A (228 mg) and 1M borane in THF (1.2 mL) in THF (2 mL) at room temperature was stirred for 5 hours, and treated sequentially with 2M sodium carbonate (1 mL) and 33% hydrogen peroxide (1 mL). The mixture was heated to 60° C. for 1 hour, diluted with ethyl acetate (1100 mL), washed with water (45 mL) and brine (110 mL), dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 20-40% ethyl acetate/hexanes to provide the desired product.

Workup

  1. washwashed with water (45 mL) and brine (110 mL)
  2. dry with materialdried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe concentrate was purified by flash column chromatography on silica gel with 20-40% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-8ef4d9e9243f448fa5cb632197406639
Source dataset
uspto-grants-2010_07
Patent number
US07754886B2

Reaction notes

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