Hydrochloric Acid → Methyl 2,2-dimethyl-3-piperidin-4-ylpropanoate hydrochloride
反応式
[CH3:1][O:2][C:3](=[O:21])[C:4]([CH3:20])([CH3:19])[CH2:5][CH:6]1[CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]1.[ClH:22]>O1CCOCC1>[ClH:22].[CH3:19][C:4]([CH3:20])([CH2:5][CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)[C:3]([O:2][CH3:1])=[O:21]参加物
4
実験手順
tert-Butyl 4-(3-methoxy-2,2-dimethyl-3-oxopropyl)piperidine-1-carboxylate (1.40 g, 4.67 mmol) was dissolved in anhydrous 4N HCl in dioxane (10 mL) and the resulting solution was stirred at rt for 1 h. The reaction mixture was concentrated to afford methyl 2,2-dimethyl-3-piperidin-4-ylpropanoate hydrochloride.
後処理
- concentrationThe reaction mixture was concentrated
出典と根拠
- ORDレコード
- ord-c3645168c6924c239b26cf6446030d71
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700591B2
反応ノート
読み込み中…