反応式
[N:1]([CH2:4][C:5]([CH2:7][N:8]=[N+:9]=[N-:10])=[O:6])=[N+:2]=[N-:3].[N-:11]=[N+:12]=[N-:13].[Na+].[CH3:15]C(C)=O>>[N:1]([CH2:4][C:5]([OH:6])([CH2:15][N:11]=[N+:12]=[N-:13])[CH2:7][N:8]=[N+:9]=[N-:10])=[N+:2]=[N-:3]参加物
4
実験手順
To a solution of 1,3-diazidoacetone 7(10 gms, 0.07 mol) in aq. acetone (20 mL water, 150 mL acetone) was added sodium azide (15 gm, 0.23 mol) and the resulting mixture was heated under reflux for 14 hours. The reaction mixture was concentrated under reduced pressure and partitioned between water and methylene chloride. The organic layer was separated, dried over sodium sulfate and concentrated to obtain a residue that was chromatographed to obtain pure 2-azidomethyl-2-hydroxy-1,3-diazidopropane 2.
後処理
- temperaturethe resulting mixture was heated
- temperatureunder reflux for 14 hours
- concentrationThe reaction mixture was concentrated under reduced pressure
- custompartitioned between water and methylene chloride
- customThe organic layer was separated
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customto obtain a residue that
- customwas chromatographed
出典と根拠
- ORDレコード
- ord-4f96268aed7f484ea1d3728519e67ad5
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06965042B1
関連ノート
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