Tributylstannane → t-Butyl 4-(2-(2-cyano-1-cyclopentanon-3-yl)ethyl]benzoate

HRID 2294096ノート

反応式

HRID 2294096 の反応式
[C:1]([C:3]1[C:4](=[O:8])[CH2:5][CH2:6][CH:7]=1)#[N:2].N(C(C)(C)C#N)=NC(C)(C)C#N.C([SnH](CCCC)CCCC)CCC.Br[CH2:35][CH2:36][C:37]1[CH:49]=[CH:48][C:40]([C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])=[CH:39][CH:38]=1>C1C=CC=CC=1>[C:1]([CH:3]1[CH:7]([CH2:35][CH2:36][C:37]2[CH:49]=[CH:48][C:40]([C:41]([O:43][C:44]([CH3:46])([CH3:45])[CH3:47])=[O:42])=[CH:39][CH:38]=2)[CH2:6][CH2:5][C:4]1=[O:8])#[N:2]

参加物

6

反応物 4

HCID 5948TributylstannaneHCID 6547AzobisisobutyronitrileHCID 10803033Tert-butyl 4-(2-bromoethyl)benzoateHCID 113893681-Cyclopentene-1-carbonitrile, 5-oxo-

生成物 1

HCID 10470833t-Butyl 4-(2-(2-cyano-1-cyclopentanon-3-yl)ethyl]benzoate

試薬・触媒・溶媒 1

HCID 241Benzene溶媒3 回

実験手順

A solution of the 2-cyano-2-cyclopenten-1-one (2.41 g, 22.5 mmol) prepared in the Preparative Example 101 in anhydrous benzene and a solution of azobisisobutyronitrile (AIBN) (0.05 g, a catalytic amount) and tri-n-butyltin hydride (3.62 g, 12.4 mmol) in anhydrous benzene were simultaneously gradually dropped into a solution of t-butyl 4-(2-bromoethyl)benzoate (3.21 g, 11.3 mmol) prepared in the Preparative Example 104 in anhydrous benzene under reflux by heating. The obtained mixture was heated under reflux for about 20 minutes and distilled to remove the solvent. The residue was purified by silica gel column chromatography to give the objective compound. yield: 0.43 g

後処理

  1. temperatureunder reflux
  2. temperatureby heating
  3. temperatureThe obtained mixture was heated
  4. temperatureunder reflux for about 20 minutes
  5. distillationdistilled
  6. customto remove the solvent
  7. customThe residue was purified by silica gel column chromatography
  8. customto give the objective compound

出典と根拠

ORDレコード
ord-e71a7fc1d19e4d69ba6a4280aac7aeca
出典データセット
uspto-grants-1997_11
特許番号
US05688800

反応ノート

読み込み中…