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Diethyl Ether → 4-(p-Chlorophenyl)-4-methyl-2-pentenal

HRID 1977708
ノート
印刷プレビュー

反応式

HRID 1977708 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:15])([CH3:14])[C:9](F)=[CH:10][C:11]#N)=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C.C([O:28]CC)C>CCCCCC.O.Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:15])([CH3:14])[CH:9]=[CH:10][CH:11]=[O:28])=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 3283Diethyl EtherHCID 21225700DiisobutylaluminumhydrideHCID 542690284-(p-Chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile

生成物 1

HCID 539399194-(p-Chlorophenyl)-4-methyl-2-pentenal収率 97%

試薬・触媒・溶媒 3

HCID 313Hydrochloric Acid溶媒HCID 962
Water
溶媒
HCID 8058Hexane溶媒

反応条件

温度
-40 °C

実験手順

A solution of 4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile, (Z)- (15.6 g, 69.7 mmol) in diethyl ether is treated dropwise with diisobutylaluminum hydride (83.6 mmol, 83.6 mL of a 1 M solution in hexane) over 90 minutes at −45° C. under nitrogen, stirred at −40° C. for 35 minutes, and diluted sequentially with water and 2 N hydrochloric acid at −10° C. The resultant aqueous mixture is stirred at room temperature for one hour and extracted with diethyl ether. The organic extracts are combined, washed sequentially with water, 2 N hydrochloric acid and water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title product as a brown oil (15.34 g, 97% yield).

後処理

  1. stirringThe resultant aqueous mixture is stirred at room temperature for one hour
  2. extractionextracted with diethyl ether
  3. washwashed sequentially with water, 2 N hydrochloric acid and water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-d1d690cf15a54aa98fa6cc357245cfca
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06235754B1

反応ノート

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