Ethylene → 4'-Methyl-5-thiazol-2-yl-biphenyl-3-carboxylic acid methyl ester

HRID 506611ノート

反応式

HRID 506611 の反応式
BrCCBr.C=C.C[Si](Cl)(C)C.Br[C:13]1[S:14][CH:15]=[CH:16][N:17]=1.[CH3:18][O:19][C:20]([C:22]1[CH:23]=[C:24]([C:29]2[CH:34]=[CH:33][C:32]([CH3:35])=[CH:31][CH:30]=2)[CH:25]=[C:26](I)[CH:27]=1)=[O:21]>C1COCC1.[Zn].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:18][O:19][C:20]([C:22]1[CH:23]=[C:24]([C:29]2[CH:30]=[CH:31][C:32]([CH3:35])=[CH:33][CH:34]=2)[CH:25]=[C:26]([C:13]2[S:14][CH:15]=[CH:16][N:17]=2)[CH:27]=1)=[O:21]

参加物

9

反応物 5

HCID 6325EthyleneHCID 6397ChlorotrimethylsilaneHCID 78391,2-DibromoethaneHCID 764302-BromothiazoleHCID 578515885-Iodo-4'-methyl-biphenyl-3-carboxylic acid methyl ester

生成物 1

HCID 594325714'-Methyl-5-thiazol-2-yl-biphenyl-3-carboxylic acid methyl ester収率 80%

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 178418397HCID 178418397、化合物触媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred suspension of zinc dust (3.06 g, 46.86 mmol) in THF (15 ml) was added 1,2-dibromoethane (0.327 ml, 3.83 mmol). The reaction mixture was heated until the evolution of ethylene was completed. Trimethylsilyl chloride (0.013 ml), THF (5 ml) and 2-bromothiazole (1.39 ml, 15.62 mmol) were added, and the reaction mixture was stirred for 20 minutes at room temperature. 5-Iodo-4′-methyl-biphenyl-3-carboxylic acid methyl ester (5.0 g, 14.2 mmol) and Pd(PPh3)4 (492.3 mg, 0.462 mmol) were added, and the mixture was refluxed for 14 hours. The reaction mixture was cooled in an ice bath and extracted with EtOAc, washed with saturated aqueous NH4Cl, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with hexanes-ethyl acetate (1:6), giving 4′-methyl-5-thiazol-2-yl-biphenyl-3-carboxylic acid methyl ester as a light yellow solid (0.42 g, 80%). MS (M+H)=310.

後処理

  1. temperaturethe mixture was refluxed for 14 hours
  2. temperatureThe reaction mixture was cooled in an ice bath
  3. extractionextracted with EtOAc
  4. washwashed with saturated aqueous NH4Cl, brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by flash column chromatography on silica gel
  9. washeluting with hexanes-ethyl acetate (1:6)

出典と根拠

ORDレコード
ord-2bffc296fe3e44eca259272b68054e5f
出典データセット
uspto-grants-2010_08
特許番号
US07786110B2

反応ノート

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