Sodium bis(trimethylsilyl)amide → 3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl ester

HRID 2117522

反応式

HRID 2117522 の反応式
[CH3:1][O:2][C:3](=[O:14])[CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]#[N:13])[CH:7]=1.[CH3:15][Si]([N-][Si](C)(C)C)(C)C.[Na+].C([O-])(O)=O.[Na+].O>C1COCC1>[CH3:1][O:2][C:3](=[O:14])[CH:4]([CH3:15])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]#[N:13])[CH:7]=1

参加物

5

反応物 3

HCID 2724254Sodium bis(trimethylsilyl)amideHCID 20257048Methyl 3-(3-cyanophenyl)propanoateHCID 86585896Sodium bicarbonate water

生成物 1

HCID 545230243-(3-Cyano-phenyl)-2-methyl-propionic acid methyl ester収率 26.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 3-(3-cyano-phenyl)-propionic acid methyl ester of Step A (220mg, 1.16 mmol) in THF (5 mL) at -78° C. was added sodium bis(trimethylsilyl)amide (1M in THF, 1.2 mL, 1.2 mmol). The reaction was stirred for 0.5 h and Mel (0.08 mL, 1.28 mmol) was added. After 1 h, a solution of saturated NaHCO3:water (1:1) was added and the reaction was warmed to room temperature. The aqueous solution was washed with CH2Cl2 (3×) and the combined organic solutions were dried (MgSO4), filtered, and concentrated. Medium pressure chromatography (6:1 hexanes:EtOAc) provided the title compound of Step B as a colorless oil (62 mg). 1H NMR (400 MHz, CDCl3) δ 7.50-7.34 (m, 4H), 3.62 (s, 3H), 3.01 (m, 1H), 2.71 (m, 2H), 1.16 (d, 3H).

後処理

  1. additionMel (0.08 mL, 1.28 mmol) was added
  2. waitAfter 1 h
  3. washThe aqueous solution was washed with CH2Cl2 (3×)
  4. dry with materialthe combined organic solutions were dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-6df66d2b183b4ca0a1b98dd1a4343ada
出典データセット
uspto-grants-2008_10
特許番号
US07442702B2

関連ノート

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