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Ethanol → 7-(4-Methylphenyl)-1,2,3,4-tetrahydroisoquinoline

HRID 1169366
ノート
印刷プレビュー

反応式

HRID 1169366 の反応式
Br[C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][N:8](C(=O)C(F)(F)F)[CH2:9]2)=[CH:4][CH:3]=1.[CH3:18][C:19]1[CH:24]=[CH:23][C:22](OB(O)O)=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+].C(O)C>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.C1(C)C=CC=CC=1>[CH3:18][C:19]1[CH:24]=[CH:23][C:22]([C:2]2[CH:11]=[C:10]3[C:5]([CH2:6][CH2:7][NH:8][CH2:9]3)=[CH:4][CH:3]=2)=[CH:21][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 702EthanolHCID 11430Potassium CarbonateHCID 109688311-(7-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)-2,2,2-trifluoroethanoneHCID 190353504-Methylphenyl dihydrogen borate

生成物 1

HCID 229900677-(4-Methylphenyl)-1,2,3,4-tetrahydroisoquinoline収率 73.3%

試薬・触媒・溶媒 2

HCID 178418397
HCID 178418397、化合物
触媒
HCID 1140Toluene溶媒

実験手順

To 7-bromo-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline (8.1 g), 4-methylphenylboric acid (3.9 g), a 2 M aqueous solution of potassium carbonate (40 ml) and ethanol (40 ml) was added toluene (100 ml), and the resulting mixture was stirred at room temperature under an argon atmosphere for 30 minutes. Thereto was added tetrakis(triphenylphosphine)palladium (1.26 g), and the resulting mixture was refluxed under an argon atmosphere for 4.5 hours. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and an aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate. After evaporation of the solvent under reduced pressure, methanol (200 ml) and a 2 M aqueous solution of potassium carbonate (50 ml) were added to the residue, and the resulting mixture was stirred overnight at room temperature. After concentration, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and was then back-extracted with 1 N hydrochloric acid. The aqueous layer was made alkaline with a 1 N aqueous solution of sodium hydroxide, was then saturated with sodium chloride and was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with anhydrous magnesium sulfate. The resulting organic layer was evaporated under reduced pressure to remove the solvent to obtain 7-(4-methylphenyl)-1,2,3,4-tetrahydroisoquinoline (4.2 g) as colorless crystals.

後処理

  1. temperaturethe resulting mixture was refluxed under an argon atmosphere for 4.5 hours
  2. extractionThe reaction mixture was extracted with ethyl acetate
  3. washthe organic layer was washed with water
  4. dry with materialan aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate
  5. customAfter evaporation of the solvent under reduced pressure, methanol (200 ml)
  6. additiona 2 M aqueous solution of potassium carbonate (50 ml) were added to the residue
  7. stirringthe resulting mixture was stirred overnight at room temperature
  8. concentrationAfter concentration
  9. extractionthe reaction mixture was extracted with ethyl acetate
  10. washThe organic layer was washed with water
  11. extractionwas then back-extracted with 1 N hydrochloric acid
  12. extractionsaturated with sodium chloride and was extracted with ethyl acetate
  13. washThe organic layer was washed with an aqueous saturated solution of sodium chloride
  14. dry with materialwas dried with anhydrous magnesium sulfate
  15. customThe resulting organic layer was evaporated under reduced pressure
  16. customto remove the solvent

出典と根拠

ORDレコード
ord-3af46dda30ce4baf9065ccca90d2743f
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06627651B1

反応ノート

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