Water → HCID 19048059, compound

HRID 1037605Notes

Reaction equation

HRID 1037605 reaction equation
[N+]([O-])([O:3][CH2:4][C:5](=[O:14])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([I:13])=[CH:9][CH:8]=1)=O.O.O.O.C([O-])(=O)C.[Na+].O>CS(C)=O>[I:13][C:10]1[CH:9]=[CH:8][C:7]([CH2:6][C:5](=[O:14])[CH:4]=[O:3])=[CH:12][CH:11]=1

Participants

5

Procedure

3-(4-Iodophenyl)-2-oxopropyl nitrate (17) (450 mg) was dissolved in dimethylsulfoxide (20 mL) and to this was added sodium acetate trihydrate (211 mg, 1.55 mmol), and stirred for an hour at room temperature. To this was added water and the product was extracted with diethyl ether (×3). The organic layer was washed sequentially with water (×1), saturated aqueous solution of sodium bicarbonate (×1) and saturated brine (×1), and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to give 3-(4-iodophenyl)-2-oxopropanal (18) as an orange solid (346 mg, <1.26 mmol, <90.1%), which was used in the next reaction without further purification.

Workup

  1. extractionthe product was extracted with diethyl ether (×3)
  2. washThe organic layer was washed sequentially with water (×1), saturated aqueous solution of sodium bicarbonate (×1) and saturated brine (×1)
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationAfter filtration
  5. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-87f0b5b1bbf7423c88a203ee6f886b1f
Source dataset
uspto-grants-2013_10
Patent number
US08546568B2

Reaction notes

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