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N-bromobutanimide → Methyl 5-phthalimidomethyl-2-nitrobenzoate

HRID 862598
ノート
印刷プレビュー

反応式

HRID 862598 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].BrN1C(=O)CCC1=O.[C:23]1(=[O:33])[NH:27][C:26](=[O:28])[C:25]2=[CH:29][CH:30]=[CH:31][CH:32]=[C:24]12.[K]>C(Cl)(Cl)(Cl)Cl.[Cl-].[Na+].O.N(C(C)(C)C#N)=NC(C)(C)C#N>[C:23]1(=[O:33])[N:27]([CH2:1][C:2]2[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=2)[C:7]([O:9][CH3:10])=[O:8])[C:26](=[O:28])[C:25]2=[CH:29][CH:30]=[CH:31][CH:32]=[C:24]12
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 67184N-bromobutanimideHCID 3314122Methyl 5-methyl-2-nitrobenzoateHCID 24194345Phthalimide potassium salt

生成物 1

HCID 19698369Methyl 5-phthalimidomethyl-2-nitrobenzoate収率 130.6%

試薬・触媒・溶媒 3

HCID 6547Azobisisobutyronitrile触媒
HCID 5943
Carbon Tetrachloride
溶媒
HCID 57417360Sodium chloride; water溶媒

反応条件

温度
50 °C

実験手順

A mixture of methyl 5-methyl-2-nitrobenzoate (35.0 g, 179 mmol), N-bromosuccinimide (33.5 g, 188 mmol), and azobisisobutyronitrile (500 mg) in carbon tetrachloride (450 mL) was refluxed for 14 h. The insoluble material formed was removed by filtration and the filtrate was concentrated. The residue was dissolved in DMF (300 mL) and potassium phthalimide (19.41 g, 45 mmol) was added. The mixture was stirred for 2 h at 50° C., poured into brine, and extracted with a 1:1 mixture of toluene and ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 4:1 to 2:1 hexane/ethyl acetate to give 20.0 g of the title compound (33%).

後処理

  1. temperaturewas refluxed for 14 h
  2. customThe insoluble material formed
  3. customwas removed by filtration
  4. concentrationthe filtrate was concentrated
  5. dissolutionThe residue was dissolved in DMF (300 mL)
  6. extractionextracted with a 1:1 mixture of toluene and ethyl acetate
  7. washThe organic layers were washed with brine
  8. dry with materialdried over magnesium sulfate
  9. concentrationconcentrated
  10. customThe residue was purified by silica gel column chromatography with 4:1 to 2:1 hexane/ethyl acetate

出典と根拠

ORDレコード
ord-448899815c6c4c8e8c828bd8678dbe6d
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05719152

反応ノート

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