Tetrahydrofuran → HCID 131731270、化合物
反応式
[I-:1].[La+3:2].[I-].[I-].[C:5]([C:9]1[N-:10][C:11]([C:19]([CH3:23])([CH3:22])[CH2:20][CH3:21])=[C:12]([C:14]([CH3:18])([CH3:17])[CH2:15][CH3:16])[N:13]=1)([CH3:8])([CH3:7])[CH3:6].[K+].[CH2:25]1[CH2:29][O:28][CH2:27][CH2:26]1>>[O:28]1[CH2:29][CH2:25][CH2:26][CH2:27]1.[O:28]1[CH2:29][CH2:25][CH2:26][CH2:27]1.[I-:1].[I-:1].[C:5]([C:9]1[N-:13][C:12]([C:14]([CH3:17])([CH3:18])[CH2:15][CH3:16])=[C:11]([C:19]([CH3:23])([CH3:22])[CH2:20][CH3:21])[N:10]=1)([CH3:8])([CH3:7])[CH3:6].[La+3:2]参加物
4
実験手順
Lanthanum (III) iodide (1.0 g, 0.002 mol) was stirred in 50 mL of THF for 30 mins at room temperature. Potassium 2-tert-butyl-4,5-di-(1,1-dimethylpropyl)imidazolate (0.6 g, 0.002 mol) was added, and the resulting mixture was refluxed for 60 hours. THF was removed by vacuum, followed by hexane extraction, then filtration. The hexane was removed by vacuum, and the resulting solid was crystallized to isolate the final product.
後処理
- temperaturethe resulting mixture was refluxed for 60 hours
- customTHF was removed by vacuum
- extractionfollowed by hexane extraction
- filtrationfiltration
- customThe hexane was removed by vacuum
- customthe resulting solid was crystallized
出典と根拠
- ORDレコード
- ord-cce2f2d0864142b2a49bae8972b66b50
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08680289B2
反応ノート
読み込み中…