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Methyl iodide → 2,2-Dimethyl-5-methoxy-6,7-dichloro-1-indanone

HRID 597001
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HRID 597001 반응식
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[C:5]([Cl:14])[C:6]([Cl:13])=[C:7]([O:11][CH3:12])[CH:8]=2)[C:3]1=[O:15].[H-].[Na+].[CH3:18]I>COCCOC>[CH3:1][C:2]1([CH3:18])[CH2:10][C:9]2[C:4](=[C:5]([Cl:14])[C:6]([Cl:13])=[C:7]([O:11][CH3:12])[CH:8]=2)[C:3]1=[O:15]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 123955612-Methyl-5-methoxy-6,7-dichloro-1-indanone

생성물 1

HCID 123955652,2-Dimethyl-5-methoxy-6,7-dichloro-1-indanone

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

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온도
30 °C

실험 절차

A stirred suspension of 2-methyl-5-methoxy-6,7-dichloro-1-indanone (12.2 g., 0.05 mole) and sodium hydride (1.43 g., 0.06 mole) in anhydrous 1,2-dimethoxyethane (500 ml.) is heated in an inert atmosphere at 80°-85° C. for 1 hour, cooled to 30° C. and treated with methyl iodide (8 ml.). The reaction mixture is refluxed for 15 minutes, then the solvent is distilled at reduced pressure. The crude product is poured into water (500 ml.), extracted into ether, washed with water and dried over magnesium sulfate. After evaporation of the ether the product is crystallized from methylcyclohexane affording 8.2 g. of 2,2-dimethyl-5-methoxy-6,7-dichloro-1-indanone which melts at 142° C.

후처리

  1. temperatureis heated in an inert atmosphere at 80°-85° C. for 1 hour
  2. temperatureThe reaction mixture is refluxed for 15 minutes
  3. distillationthe solvent is distilled at reduced pressure
  4. additionThe crude product is poured into water (500 ml.)
  5. extractionextracted into ether
  6. washwashed with water
  7. dry with materialdried over magnesium sulfate
  8. customAfter evaporation of the ether the product
  9. customis crystallized from methylcyclohexane affording 8.2 g

출처 및 근거

ORD 기록
ord-2fc18d7ed3d24f8ab8be433b7baf09d7
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04012524

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