反応式
C[Si](C)(C)N[Si](C)(C)C.[Li].[C:11]([CH2:16][S:17][CH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=1)([O:13][CH2:14][CH3:15])=[O:12].I[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]Cl.CN1CCCN(C)C1=O>O1CCCC1>[C:11]([C:16]1([S:17][CH2:18][C:19]2[CH:20]=[CH:21][C:22]([O:25][CH3:26])=[CH:23][CH:24]=2)[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1)([O:13][CH2:14][CH3:15])=[O:12]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- -78 °C
実験手順
Cool lithium hexamethyldisilazane (8.4 mL of a 1.0M solution in tetrahydrofuran, 8.4 mmol) to -78° C. Add, by cannula transfer, a solution of 1-(carboethoxy)-1-(4-methoxybenzylthio)methane (2.0 g, 8.3 mmol) in tetrahydrofuran (8 mL). Stir for 45 minutes then add a solution of 1-iodo-5-chloropentane (1.94 g, 8.32 mmol) i n tetrahydrofuran (8 mL). Stir for 1 hour and add 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) (1.21 mL, 10.0 mmol). Stir at 0° C. for 4 hours and at room temperature for 6 hours. Cool to -78° C., add lithium hexamethyldisilazane (8.4 mL, 8.4 mmol) and stir at room temperature overnight. Quench with saturated ammonium chloride (5 mL) and partition between ethyl acetate (50 mL) and water (50 mL). Separate the organic phase, dry (Na2SO4) and evaporate the solvent in vacuo. Purify by chromatography (6:1 hexane/ethyl acetate) to give 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane as an colorless oil (1.45 g, 56%).
後処理
- additionAdd, by cannula transfer
- stirringStir for 1 hour
- stirringStir at 0° C. for 4 hours and at room temperature for 6 hours
- stirringstir at room temperature overnight
- customQuench with saturated ammonium chloride (5 mL)
- custompartition between ethyl acetate (50 mL) and water (50 mL)
- customSeparate the organic phase
- dry with materialdry (Na2SO4)
- customevaporate the solvent in vacuo
- customPurify by chromatography (6:1 hexane/ethyl acetate)
出典と根拠
- ORDレコード
- ord-78f6d88fed804c71b14c5ce3a9b19d24
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05428158
関連ノート
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