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HCID 141711、化合物 → Benzaldehyde, p-phenethyl-

HRID 962630
ノート
印刷プレビュー

反応式

HRID 962630 の反応式
[C:1]1([CH:9]=[CH:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:6]=[CH:5][C:4]([CH:7]=[O:8])=[CH:3][CH:2]=1>C(OCC)(=O)C.[Pd]>[CH2:9]([C:1]1[CH:2]=[CH:3][C:4]([CH:7]=[O:8])=[CH:5][CH:6]=1)[CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 141711HCID 141711、化合物

生成物 1

HCID 121060Benzaldehyde, p-phenethyl-収率 50.5%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 4-stilbenecarboxaldehyde (5.14 g, 24.68 mmol) in 125 mL of ethyl acetate was added 0.13 g of 5% Pd/C catalyst. The reaction was stirred under hydrogen (1 atm) for 2 hours. An additional 0.14 g of 5% Pd/C catalyst was added and the reaction mixture was stirred under hydrogen (1 atm) again for 1 hour. The catalyst was removed by filtration through a pad of Celite. The residue was washed with ethyl acetate (2×30 mL) and the filtrate was concentrated on a rotavap. The residue oil was chromatographed with 15% ethyl acetate in hexanes on silica gel to give 2.62 g (50%) of the desired product as a white solid.

後処理

  1. stirringthe reaction mixture was stirred under hydrogen (1 atm) again for 1 hour
  2. customThe catalyst was removed by filtration through a pad of Celite
  3. washThe residue was washed with ethyl acetate (2×30 mL)
  4. concentrationthe filtrate was concentrated on a rotavap
  5. customThe residue oil was chromatographed with 15% ethyl acetate in hexanes on silica gel

出典と根拠

ORDレコード
ord-9669dbadd90a46f6b459ea6c42f43826
出典データセット
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05760048

反応ノート

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