Lithium Hydroxide → 2-(Cyclohexylmethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid
反応式
[CH:1]1([CH2:7][CH:8]2[CH2:13][CH:12]([C:14]([O:16]C)=[O:15])[CH2:11][CH2:10][N:9]2[C:18]([O:20][CH3:21])=[O:19])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Li+].[OH-]>C1COCC1.O>[CH:1]1([CH2:7][CH:8]2[CH2:13][CH:12]([C:14]([OH:16])=[O:15])[CH2:11][CH2:10][N:9]2[C:18]([O:20][CH3:21])=[O:19])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1参加物
実験手順
Dimethyl 2-(cyclohexylmethyl)piperidine-1,4-dicarboxylate (2.20 g, 7.40 mmol) was dissolved in THF (25 mL) and water (25 mL). LiOH (0.266 g, 11.1 mmol) was added and the resulting mixture was stirred at room temperature overnight and heated under reflux for 30 min. The reaction mixture was partitioned between 1 M KHSO4 and diethyl ether. The organic phase was dried (Na2SO4), filtered through Celite® and the solvent was evaporated. The crude product was dissolved again in THF (25 mL) and water (25 mL). LiOH (0.23 g) was added to the reaction flask. The reaction mixture was stirred overnight. The reaction was worked up as above to give the product. 1H NMR (600 MHz, cdcl3) δ 0.85 (ddd, 2H), 1.19 (dddd, 5H), 1.38-1.48 (m, 1H), 1.61 (d, 4H), 1.72 (tt, 2H), 1.97 (qd, 3H), 2.56-2.65 (m, 1H), 3.02-3.14 (m, 1H), 3.67 (d, 3H), 3.88 (d, 1H), 4.22 (s, 1H).
後処理
- temperatureheated
- temperatureunder reflux for 30 min
- customThe reaction mixture was partitioned between 1 M KHSO4 and diethyl ether
- dry with materialThe organic phase was dried (Na2SO4)
- filtrationfiltered through Celite®
- customthe solvent was evaporated
- dissolutionThe crude product was dissolved again in THF (25 mL)
- additionLiOH (0.23 g) was added to the reaction flask
- stirringThe reaction mixture was stirred overnight
- customto give the product
出典と根拠
- ORDレコード
- ord-575fbe7982bb4b10ab8da3783db3f2bd
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08415378B2
反応ノート
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