Acetic Acid → HCID 44377347, compound

HRID 2370650Notes

Reaction equation

HRID 2370650 reaction equation
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=O.[CH2:11]([NH:13][CH2:14][CH3:15])[CH3:12].[B-]C#N.[Na+].C(O)(=O)C>CO>[CH2:11]([N:13]([CH2:14][CH3:15])[CH:2]1[CH2:3][C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1]1)[CH3:12]

Participants

6

Procedure

To a solution of 1H-inden-2(3H)-one (6.00 g, 45.4 mmol) in methanol (100 ml) was added diethylamine (6.64 g, 91 mmol), sodium cyanotrihydroborate (5.71 g, 91 mmol) and acetic acid (5.45 g, 91 mmol). The reaction mixture was stirred overnight and concentrated. The residue was diluted with methylene chloride, washed with saturated aqueous NaHCO3 (2×50 mL), dried over Na2SO4, filtered, and concentrated. The resulting residue was dissolved in 1M aqueous HCl (100 ml), and extracted with methylene chloride (2×50 mL). The aqueous layer was treated with 6N aqueous NaOH solution until the pH=14 and was extracted with methylene chloride (4×100 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated to provide the title compound.

Workup

  1. concentrationconcentrated
  2. additionThe residue was diluted with methylene chloride
  3. washwashed with saturated aqueous NaHCO3 (2×50 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe resulting residue was dissolved in 1M aqueous HCl (100 ml)
  8. extractionextracted with methylene chloride (2×50 mL)
  9. additionThe aqueous layer was treated with 6N aqueous NaOH solution until the pH=14
  10. extractionwas extracted with methylene chloride (4×100 mL)
  11. dry with materialThe combined organic layers were dried over Na2SO4
  12. filtrationfiltered
  13. concentrationconcentrated

Sources & evidence

ORD record
ord-110d962b4c8545b7a09366949444b47e
Source dataset
uspto-grants-2014_04
Patent number
US08710065B2

Reaction notes

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