Allyl Alcohol → 2-Chloro-5(3-oxopropyl)-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide

HRID 719639ノート

反応式

HRID 719639 の反応式
[Cl:1][C:2]1[CH:21]=[CH:20][C:19](I)=[CH:18][C:3]=1[C:4]([NH:6][CH2:7][C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2)=[O:5].C(=O)([O-])O.[Na+].[CH2:28]([OH:31])[CH:29]=[CH2:30]>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.CC([O-])=O.CC([O-])=O.[Pd+2].C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:21]=[CH:20][C:19]([CH2:30][CH2:29][CH:28]=[O:31])=[CH:18][C:3]=1[C:4]([NH:6][CH2:7][C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2)=[O:5]

参加物

7

反応条件

温度
80 °C

実験手順

2-Chloro-5-iodo-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (5.00 g, Example 14a), tetrabutylammonium chloride (3.40 g) and sodium hydrogencarbonate (2.44 g) were charged to a flask. Pd(OAc)2 (0.0533 g), toluene (50 ml) and allyl alcohol (1.01 ml) were added to afford a pale brown mixture which was heated at 80° C. for 5 h. The resulting dark brown mixture was cooled to ambient then filtered to remove the solid residues. These were washed with further toluene (2×50 ml) and the combined toluene extracts then washed with water (100 ml), dried over MgSO4 and concentrated to a light brown solid (3.82 g).

後処理

  1. customto afford a pale brown mixture which
  2. temperatureThe resulting dark brown mixture was cooled
  3. filtrationto ambient then filtered
  4. customto remove the solid residues
  5. washThese were washed with further toluene (2×50 ml)
  6. washthe combined toluene extracts then washed with water (100 ml)
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated to a light brown solid (3.82 g)

出典と根拠

ORDレコード
ord-e6564fcce9604abd80a7b0be0ef1357e
出典データセット
uspto-grants-2006_11
特許番号
US07132457B2

反応ノート

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