N-bromobutanimide → 2,8-dimethyl-5H-dibenzo[a,d][7]annulen-5-one

HRID 1275901ノート

反応式

HRID 1275901 の反応式
[CH3:1][C:2]1[CH:18]=[CH:17][C:5]2[C:6](=[O:16])[C:7]3[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:8]=3[CH2:9][CH2:10][C:4]=2[CH:3]=1.BrN1C(=O)CCC1=O>C(OCC)(=O)C>[CH3:1][C:2]1[CH:18]=[CH:17][C:5]2[C:6](=[O:16])[C:7]3[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:8]=3[CH:9]=[CH:10][C:4]=2[CH:3]=1

参加物

4

反応物 2

HCID 67184N-bromobutanimideHCID 2211720110,11-dihydro-2,8-dimethyl-5H-dibenzo[a,d]cyclohepten-5-one

生成物 1

HCID 221172592,8-dimethyl-5H-dibenzo[a,d][7]annulen-5-one

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

10,11-Dihydro-2,8-dimethyl-5H-dibenzo[a,d]cyclohepten-5-one (European Patent, 1993, 0 25 589 322 A1) (6 g) and N-bromosuccinimide (5 g) in ethyl acetate (100 ml) was irradiated with a 500 W halogen lamp. After 5 hours the reaction mixture was cooled and quenched with brine. The organic layer was collected, dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in dry dimethylformamide, treated with 1,5-diazabicyclo[4.3.0]non-5-ene (3.5 ml) and heated at 80° C. for 0.25 hours. The cooled reaction mixture was washed with 2M HCl, brine, dried (MgSO4) and evaporated under reduced pressure. Purification was by chromatography eluting with toluene. Yield 4.5 g.

後処理

  1. temperatureAfter 5 hours the reaction mixture was cooled
  2. customquenched with brine
  3. customThe organic layer was collected
  4. dry with materialdried (MgSO4)
  5. customevaporated under reduced pressure
  6. dissolutionThe residue was dissolved in dry dimethylformamide
  7. additiontreated with 1,5-diazabicyclo[4.3.0]non-5-ene (3.5 ml)
  8. customThe cooled reaction mixture
  9. washwas washed with 2M HCl, brine
  10. dry with materialdried (MgSO4)
  11. customevaporated under reduced pressure
  12. customPurification
  13. washeluting with toluene

出典と根拠

ORDレコード
ord-458b634a76da4bd4b11ba3c01f990cd4
出典データセット
uspto-grants-2000_12
特許番号
US06162808

反応ノート

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