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4-(Cyclopropylmethyl)benzaldehyde → HCID 19010837, 화합물

HRID 1741831
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HRID 1741831 반응식
[CH2:1]([Mg]Br)[CH:2]=[CH2:3].[CH:6]1([CH2:9][C:10]2[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=2)[CH2:8][CH2:7]1>C(OCC)C>[CH:6]1([CH2:9][C:10]2[CH:11]=[CH:12][C:13]([CH:14]([OH:15])[CH2:3][CH:2]=[CH2:1])=[CH:16][CH:17]=2)[CH2:8][CH2:7]1
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참가 물질

4

반응물 2

HCID 190108254-(Cyclopropylmethyl)benzaldehydeHCID 178455850HCID 178455850, 화합물

생성물 1

HCID 19010837HCID 19010837, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a solution of allylmagnesium bromide (1.0M in diethyl ether, 3 ml) in diethyl ether (5 ml) was added dropwise 4-(cyclopropylmethyl)benzaldehyde (240 mg) in diethyl ether (2 ml) at 0° C. After 15 minutes, the reaction mixture was quenched by aqueous ammonium chloride and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel column eluting with a mixture of hexane and ethyl acetate (85:15) to give 1-[4-(cyclopropylmethyl)phenyl]-3-buten-1-ol (229 mg) as an oil.

후처리

  1. customthe reaction mixture was quenched by aqueous ammonium chloride
  2. extractionthe resulting mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was chromatographed on silica gel column
  7. washeluting with a mixture of hexane and ethyl acetate (85:15)

출처 및 근거

ORD 기록
ord-44ce09d171884f7296faad4eddb0ccbd
출처 데이터셋
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05334716

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