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Ethanol → 4-Isobutylbenzaldehyde oxime

HRID 2247678
ノート
印刷プレビュー

反応式

HRID 2247678 の反応式
[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].C(O)C.N1C=CC=CC=1.Cl.[NH2:23][OH:24]>CCOCC.O>[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[N:23][OH:24])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 702EthanolHCID 1049PyridineHCID 443297Hydroxyamine hydrochlorideHCID 577537Benzaldehyde, 4-(2-methylpropyl)-

生成物 1

HCID 802569644-Isobutylbenzaldehyde oxime収率 84%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 3283
Diethyl Ether
溶媒

実験手順

To a solution of 4-isobutylbenzaldehyde (5.0 g, 31 mmol) in a mixed solvent of ethanol (25 ml) and pyridine (25 ml) was added hydroxylamine hydrochloride (2.4 g, 34 mmol) with stirring, and the resulting mixture was stirred at room temperature for 18 hours. After evaporating the reaction mixture in vacuo, the residue thus obtained was diluted with ether, poured into water (150 ml) and extracted with ether. The extract was washed successively with 1N hydrochloric acid and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:19 to 1:9) as the eluent to afford the title compound (4.6 g) in a yield of 84% as a colourless oily product.

後処理

  1. stirringthe resulting mixture was stirred at room temperature for 18 hours
  2. customAfter evaporating the reaction mixture in vacuo
  3. customthe residue thus obtained
  4. extractionextracted with ether
  5. washThe extract was washed successively with 1N hydrochloric acid
  6. dry with materiala saturated aqueous solution of sodium chloride and dried over magnesium sulfate
  7. filtrationAfter filtration
  8. customthe filtrate was evaporated in vacuo

出典と根拠

ORDレコード
ord-d46253ce467a462ebd250c6065799f66
出典データセット
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07687491B2

反応ノート

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