Methyl Benzoate → 4-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl ester

HRID 33864

反応式

HRID 33864 の反応式
[CH3:1][O:2][C:3](=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[H-].[Na+].[N:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][C:14]=1[CH:23]=O.[CH2:25]1COCC1>C(O)C.[OH-].[Pd+2].[OH-]>[CH3:1][O:2][C:3](=[O:10])[C:4]1[CH:9]=[CH:8][C:7]([CH2:25][CH2:23][C:14]2[CH:15]=[CH:16][C:17]3[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=3)[N:13]=2)=[CH:6][CH:5]=1

参加物

7

反応物 4

HCID 7150Methyl BenzoateHCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 796192-Quinolinecarboxaldehyde

生成物 1

HCID 685758694-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl ester

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒HCID 702Ethanol溶媒

実験手順

To a solution of 4-[Triphenyl-phophanyl)-methyl]-benzoic acid methyl ester (1.87 g) in THF (16 ml) under N2 atmosphere at 0° C. was added sodium hydride (165 mg (60%)). After 30 min, quinoline-2-carbaldehyde (0.50 g) was added and the reaction stirred at ambient temperature for 2 h. The reaction mixture was quenched with brine, extracted with chloroform, dried magnesium sulfate, filtered and concentrated to provide the crude alkene. The crude product was placed on a parr shaker in ethanol (15 ml) with palladium hydroxide (200 mg) as the catalyst under 10 PSI of H2. After 40 min, the reaction mixture was filtered through celite and concentrated. Biotage MPLC chromatography eluting with 10-20% ethyl acetate/hexane provided the title compound. MS: (M+H m/z=292.1).

後処理

  1. customThe reaction mixture was quenched with brine
  2. extractionextracted with chloroform, dried magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto provide the crude alkene
  6. waitAfter 40 min
  7. filtrationthe reaction mixture was filtered through celite and
  8. concentrationconcentrated
  9. washBiotage MPLC chromatography eluting with 10-20% ethyl acetate/hexane

出典と根拠

ORDレコード
ord-68e438b175834339a48d1f36eaa20468
出典データセット
uspto-grants-2008_09
特許番号
US07429665B2

関連ノート

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