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Ethanol → 4-Isobutylbenzaldehyde oxime

HRID 2247678
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HRID 2247678 반응식
[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]
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참가 물질

7

반응물 4

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

생성물 1

HCID 802569644-Isobutylbenzaldehyde oxime수율 84%

시약·촉매·용매 2

HCID 962Water용매
HCID 3283
Diethyl Ether
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d46253ce467a462ebd250c6065799f66
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687491B2

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