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Methyl iodide → HCID 60026352, 화합물

HRID 400646
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HRID 400646 반응식
[CH3:1][C:2]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([CH2:5][CH:6]=[CH2:7])[CH2:3][OH:4].[H-].[Na+].[CH3:16]I>CN(C=O)C>[CH3:16][O:4][CH2:3][C:2]([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([CH3:1])[CH2:5][CH:6]=[CH2:7]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 3019061beta-Allyl-beta-methylphenethyl alcohol

생성물 1

HCID 60026352HCID 60026352, 화합물수율 98.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 2-methyl-2-phenylpent-4-en-1-ol (3.2 g, 18.15 mmol) in 17 mL of DMF was added sodium hydride (1.25 g, 31.25 mmol, 60% in mineral oil). The mixture was stirred until foaming ceased and then methyl iodide (6 mL, 96 mmol) was added. After 2 hours, the mixture was quenched with 50 mL of saturated aqueous ammonium chloride solution and extracted with three 50 mL portions of ethyl acetate. The combined organic layers were washed with 30 mL of saturated aqueous ammonium chloride solution, five 25 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 3.4 g (98.4% yield) of (1-methoxymethyl-1-methylbut-3-enyl)benzene which was used without further purification.

후처리

  1. customthe mixture was quenched with 50 mL of saturated aqueous ammonium chloride solution
  2. extractionextracted with three 50 mL portions of ethyl acetate
  3. washThe combined organic layers were washed with 30 mL of saturated aqueous ammonium chloride solution, five 25 mL portions of brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-1759b24fe55b4439a0f5b7ed36b2830d
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08741897B2

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