Phosphorus oxychloride → 2,9-Di-tert-butyl-6-chlorophenanthridine

HRID 1097146ノート

反応式

HRID 1097146 の反応式
[C:1]([CH:5]1[CH:18]=[CH:17][C:16]2[C:7](=[C:8]3[C:13](=[CH:14][N:15]=2)[CH:12]=[CH:11][C:10]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:9]3)[C:6]1=O)([CH3:4])([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)(Cl)[Cl:25].P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[C:1]([C:5]1[CH:18]=[CH:17][C:16]2[C:7](=[C:8]3[C:13](=[C:14]([Cl:25])[N:15]=2)[CH:12]=[CH:11][C:10]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:9]3)[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]

参加物

5

反応物 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 668135942,9-Di-t-butylphenanthridinone

生成物 1

HCID 574376592,9-Di-tert-butyl-6-chlorophenanthridine収率 98%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

The above 2,9-di-t-butylphenanthridinone (3.0 g, 9.7 mmole) was added to a reaction flask containing phosphorus pentachloride (3.0 g, 14.6 mmole) and 50 mL of phosphoryl chloride. The reaction mixture was refluxed overnight, cooled to room temperature and diluted with toluene. The excess phosphoryl chloride and toluene were removed by a rotary evaporator. The residue was dissolved into ethyl acetate and washed with distilled water followed by brine. The solvent layer was dried over magnesium sulfate, filtered and concentrated to give the desired 2,9-di-tert-butyl-6-chlorophenanthridine (3.0 grams, 98%) as an off white solid. The product was confirmed by GC Mass Spec and not purified further but used directly in the next step.

後処理

  1. temperatureThe reaction mixture was refluxed overnight
  2. customThe excess phosphoryl chloride and toluene were removed by a rotary evaporator
  3. dissolutionThe residue was dissolved into ethyl acetate
  4. washwashed with distilled water
  5. dry with materialThe solvent layer was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-ec5e3501bb59436fa29c1786d24b8627
出典データセット
uspto-grants-2012_03
特許番号
US08142909B2

反応ノート

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