Acetic Anhydride → N-(4-Hydroxy-3-oxo-2,3-dihydro-1H-inden-5-yl)acetamide

HRID 1039260Notes

Reaction equation

HRID 1039260 reaction equation
Br.[NH2:2][C:3]1[C:11]([OH:12])=[C:10]2[C:6]([CH2:7][CH2:8][C:9]2=[O:13])=[CH:5][CH:4]=1.C(N(CC)CC)C.[C:21](OC(=O)C)(=[O:23])[CH3:22].C(=O)([O-])O.[Na+]>O1CCCC1>[OH:12][C:11]1[C:3]([NH:2][C:21](=[O:23])[CH3:22])=[CH:4][CH:5]=[C:6]2[C:10]=1[C:9](=[O:13])[CH2:8][CH2:7]2

Participants

6

Reactant 4

HCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 516892Sodium BicarbonateHCID 673534616-Amino-7-hydroxy-2,3-dihydro-1H-inden-1-one hydrobromide

Product 1

HCID 67354064N-(4-Hydroxy-3-oxo-2,3-dihydro-1H-inden-5-yl)acetamideYield 71.5%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

6-Amino-7-hydroxyindan-1-one hydrobromide (800 mg, 3.28 mmol) was suspended in tetrahydrofuran (20 mL), triethylamine (571 μL, 4.10 mmol) and acetic anhydride (387 μL, 4.10 mmol) were added, and the mixture was stirred at room temperature for 1.5 hr. To the reaction solution was added saturated aqueous sodium hydrogencarbonate solution. The mixture was extracted with ethyl acetate, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=60/40→100/0) to give the title compound (481 mg, yield 71%).

Workup

  1. extractionThe mixture was extracted with ethyl acetate
  2. washwashed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=60/40→100/0)

Sources & evidence

ORD record
ord-d31468b687984c19b2625354b8fb8085
Source dataset
uspto-grants-2013_10
Patent number
US08552037B2

Reaction notes

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