Ammonium Acetate → HCID 66649229, compound
Reaction equation
[F:1][C:2]1[CH:11]=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([C:13](=O)[CH3:14])=[CH:7]2.C([O-])(=O)C.[NH4+].C([BH3-])#[N:22].[Na+]>CO>[F:1][C:2]1[CH:11]=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH:13]([NH2:22])[CH3:14])=[CH:7]2Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The above ketone (760 mg, 3.689 mmol) was dissolved in methanol (40 ml). Then, ammonium acetate (2.841 g, 36.896 mmol), sodium cyanoborohydride (232 mg, 3.389 mmol) and molecular sieves (3 Å, 7.6 g) were added. The mixture was stirred at room temperature for two days. The solid was filtered and the filtrate was concentrated. The residue was dissolved in water and concentrated aqueous HCl was added dropwise until the pH≈2. The mixture was then extracted with ethyl acetate to remove the unfinished ketone and other by-products. The water layer was basified to pH≈10 with aqueous sodium hydroxide (1M), and was extracted with dichloromethane and the organic layers were combined, dried over magnesium sulfate and concentrated to afford 290 mg of 1-(5,7-difluoro-naphthalen-2-yl)-ethylamine (38% yield).
Workup
- filtrationThe solid was filtered
- concentrationthe filtrate was concentrated
- dissolutionThe residue was dissolved in water
- additionconcentrated aqueous HCl was added dropwise until the pH≈2
- extractionThe mixture was then extracted with ethyl acetate
- customto remove the unfinished ketone and other by-products
- extractionwas extracted with dichloromethane
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-4ad7e5c564644b948b6b1ccbcbb4a1fd
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063057B2
Reaction notes
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