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Isopropyl iodide → 5-chloro-2-isopropoxybenzaldehyde

HRID 1728164
ノート
印刷プレビュー

反応式

HRID 1728164 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:10])=[C:6]([CH:9]=1)[CH:7]=[O:8].I[CH:12]([CH3:14])[CH3:13].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH:12]([CH3:14])[CH3:13])=[C:6]([CH:9]=1)[CH:7]=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 124815-Chloro-salicylaldehyde

生成物 1

HCID 51996155-chloro-2-isopropoxybenzaldehyde収率 78.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

5-Chloro-2-hydroxy-benzaldehyde (3 g, 19.16 mmol),2-Iodo-propane (4.88 g, 28.74 mmol) and K2CO3 (4 g, 28.74 mmol) was mixed in anhydrous DMF. The reaction tube was placed into the cavity of a focused monomode microwave reactor and the contents of the flask were irradiated for 30 min at 100° C. Then the solution was filtered and the filtration was concentrated to obtain the crude product (3 g). The crude product was used into next step reaction without further purification.

後処理

  1. customThe reaction tube was placed into the cavity of a focused monomode microwave reactor
  2. customthe contents of the flask were irradiated for 30 min at 100° C
  3. filtrationThen the solution was filtered
  4. filtrationthe filtration
  5. concentrationwas concentrated

出典と根拠

ORDレコード
ord-831fe5f47a49478886682d089bd99e2a
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07495007B2

反応ノート

読み込み中…

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