Hydrochloric Acid → Methyl 1-isopropyl-1H-indole-6-carboxylate
反応式
CO[CH:3](OC)[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([O:13][CH3:14])=[O:12])=[CH:7][C:6]=1[NH:15][CH:16]([CH3:18])[CH3:17].Cl>CO>[C:11]([C:8]1[CH:7]=[C:6]2[C:5]([CH:4]=[CH:3][N:15]2[CH:16]([CH3:18])[CH3:17])=[CH:10][CH:9]=1)([O:13][CH3:14])=[O:12]参加物
4
実験手順
4-Carbomethoxy-2-(N-2-propylamino)phenylacetaldehyde dimethylacetal (3.7 g, 13.15 mmole) was refluxed with 100 mL of 1N hydrochloric acid in methanol for 1 h. The solution was concentrated and the residue dissolved in 50 mL of ethyl acetate, washed with saturated sodium bicarbonate solution, dried organic layer over magnesium sulfate and evaporated to give 2.78 g of 6-carbomethoxy-1-(2-propyl)indole.
後処理
- concentrationThe solution was concentrated
- dissolutionthe residue dissolved in 50 mL of ethyl acetate
- washwashed with saturated sodium bicarbonate solution, dried organic layer over magnesium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-ee653f7bebe748cdb1a83ef871bf4b78
- 出典データセット
- uspto-grants-2000_02
- 特許番号
- US06030994
反応ノート
読み込み中…