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Methyl iodide → HCID 11148076, 화합물

HRID 855899
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HRID 855899 반응식
[CH:1]([O:4][C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[O:10])=[CH:7][CH:6]=1)([CH3:3])[CH3:2].[Mg].I[CH3:15].[Cl-].[NH4+]>C(OCC)C.O>[CH:1]([O:4][C:5]1[CH:12]=[CH:11][C:8]([CH:9]([OH:10])[CH3:15])=[CH:7][CH:6]=1)([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6328Methyl iodideHCID 25517Ammonium ChlorideHCID 2500774-IsopropoxybenzaldehydeHCID 5462224Magnesium

생성물 1

HCID 11148076HCID 11148076, 화합물수율 92.5%

시약·촉매·용매 2

HCID 962Water용매
HCID 3283
Diethyl Ether
용매

실험 절차

A solution of 4-isopropyloxy benzaldehyde of formula 5 (5 g, 30 mmol) in dry diethyl ether is slowly added to an ethereal solution of Grignard reagent prepared from magnesium metal (0.84 g, 35 mmol) and iodomethane (2.6 ml, 40 mmol) and the contents stirred for 1 hour at room temperature. After the completion of the reaction, the mixture is worked up by adding saturated aqueous solution of ammonium chloride (10 ml), followed by dilution with water (100 ml), separating the organic layer and extracting the aqueous layer with solvent ether (2×100 ml). The combined organic layer is washed with water (2>20 ml), dried over anhydrous sodium sulphate and concentrated in vacuo to yield 1-(4 -isopropyloxy phenyl) ethanol, in a semisolid of general formula 4 in 92.5% yield.

후처리

  1. customAfter the completion of the reaction
  2. customseparating the organic layer
  3. extractionextracting the aqueous layer with solvent ether (2×100 ml)
  4. washThe combined organic layer is washed with water (2>20 ml)
  5. dry with materialdried over anhydrous sodium sulphate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-fcf6aebfc12e4d99a11669bf73ef5016
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262296B2

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