Acetyl chloride → 1-(7-acetyl-4,5-dihydro-1H-1,5-methanobenzo[d]azepin-3(2H)-yl)-2,2,2-trifluoroethanone

HRID 395309ノート

反応式

HRID 395309 の反応式
[CH:1]12[CH2:18][CH:8]([CH2:9][N:10]([C:12](=[O:17])[C:13]([F:16])([F:15])[F:14])[CH2:11]1)[C:7]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]2=1.[C:19](Cl)([CH3:21])=[O:20].[Cl-].[Al+3].[Cl-].[Cl-].C([O-])(O)=O.[Na+]>ClCCCl>[C:19]([C:5]1[CH:4]=[CH:3][C:2]2[CH:1]3[CH2:18][CH:8]([CH2:9][N:10]([C:12](=[O:17])[C:13]([F:15])([F:16])[F:14])[CH2:11]3)[C:7]=2[CH:6]=1)(=[O:20])[CH3:21]

参加物

6

実験手順

1-(10-Aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (253 mg, 1.0 mmol) and AcCl (0.68 mL, 10 mmol) were dissolved in DCE (3 mL) and treated with aluminum chloride (AlCl3) (667 mg, 5.0 mmol). The resulting yellow mixture was stirred for 30 minutes then poured over ice and saturated aqueous NaHCO3 solution. After stirring 20 minutes the mixture was extracted with CH2Cl2 (3×30 mL). The organic layer was dried through a cotton plug then concentrated to a orange-yellow oil (255 mg, 86%).

後処理

  1. stirringAfter stirring 20 minutes the mixture
  2. extractionwas extracted with CH2Cl2 (3×30 mL)
  3. customThe organic layer was dried through a cotton plug
  4. concentrationthen concentrated to a orange-yellow oil (255 mg, 86%)

出典と根拠

ORDレコード
ord-bfea9390f7584f24a401da01fc3aa938
出典データセット
uspto-grants-2003_08
特許番号
US06605610B1

反応ノート

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