Trifluoroacetic acid → 1-Benzyl-4-[(R)-2-(tert-butyldimethylsilyloxy)-1-(methyl)ethyl]pyrrolidine-3-carboxylic acid methyl ester
反応式
[CH2:1]([N:8]([CH2:14]OC)[CH2:9][Si](C)(C)C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Si:17]([O:24][CH2:25][C@H:26]([CH3:30])/[CH:27]=[CH:28]/[CH3:29])([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18].FC(F)(F)[C:33](O)=[O:34].O.C(=O)(O)[O-:40].[Na+]>C(Cl)Cl>[CH3:33][O:34][C:29]([CH:28]1[CH:27]([C@@H:26]([CH3:30])[CH2:25][O:24][Si:17]([C:20]([CH3:21])([CH3:22])[CH3:23])([CH3:19])[CH3:18])[CH2:9][N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:14]1)=[O:40]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine (16.6 mL, 65.0 mmol) was added to a solution of (E)-(R)-5-(tert-butyldimethylsilyloxy)-4-methylpent-2-ene acid methyl ester (14 g, 54.2 mmol) in methylene chloride (100 mL), and then a trace amount of trifluoroacetic acid was added. The mixture was stirred for 30 minutes and then saturated sodium bicarbonate water was added. The organic layer was separated and dried over magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give 14.6 g (69%) of the diastereomer mixture title compound as a colorless oil. The diastereomers were used for the next step without separation.
後処理
- customThe organic layer was separated
- dry with materialdried over magnesium sulfate
- filtrationAfter filtration
- customthe solvent was evaporated under reduced pressure
- customthe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1)
出典と根拠
- ORDレコード
- ord-5cf4918330174b1286454efde22d1e20
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08618094B2
反応ノート
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