Carbon Dioxide → HCID 18509459、化合物
反応式
[CH3:1][C:2]([CH3:20])([CH3:19])[C:3]#[C:4]/[CH:5]=[CH:6]/[CH2:7][N:8]([CH2:10][C:11]1[CH:16]=[C:15](Br)[CH:14]=[CH:13][C:12]=1[CH3:18])[CH3:9].C(=O)=[O:22].[CH2:24]([Li])[CH2:25][CH2:26]C.CCCCCC.[Cl-].[NH4+]>O1CCCC1.CC(C)=O>[CH3:1][C:2]([CH3:20])([CH3:19])[C:3]#[C:4]/[CH:5]=[CH:6]/[CH2:7][N:8]([CH2:10][C:11]1[CH:16]=[C:15]([C:25]([OH:22])([CH3:26])[CH3:24])[CH:14]=[CH:13][C:12]=1[CH3:18])[CH3:9]参加物
実験手順
Compound 32 (1.10 g) was dissolved in tetrahydrofuran (10 ml), and the solution was cooled to −78° C. by use of a mixture of dry ice and acetone solvent. n-butyl lithium in n-hexane (1.63 M: 2.1 ml; 1.04 eq) was slowly added dropwise to the mixture, and stirred for 5 minutes, followed by dropwise addition of acetone (290 μl; 1.2 eq). The mixture was stirred for 15 minutes, and gradually brought to room temperature. Saturated aqueous ammonium chloride solution was added dropwise to the mixture, and the reaction was stopped, followed by extraction with ether (120 ml). The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane ethyl acetate=5:1), to thereby yield 520 mg of the target compound (yield: 50.4%).
後処理
- stirringThe mixture was stirred for 15 minutes
- customgradually brought to room temperature
- extractionfollowed by extraction with ether (120 ml)
- dry with materialThe organic layer was dried over magnesium sulfate
- customthe solvent was evaporated under reduced pressure
- customThe residue was purified by silica gel column chromatography (n-hexane ethyl acetate=5:1)
出典と根拠
- ORDレコード
- ord-15d24c5c6da54940b6424bde7915f0dc
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06586633B1
反応ノート
読み込み中…