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2,5-Dimethyl-4-(3,5-dimethylphenyl)indene → Lithium[2,5-dimethyl-4-(3,5-dimethylphenyl)indenide]

HRID 1372542
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HRID 1372542 반응식
[CH3:1][C:2]1[CH2:3][C:4]2[C:9]([CH:10]=1)=[C:8]([C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[C:13]([CH3:18])[CH:12]=1)[C:7]([CH3:19])=[CH:6][CH:5]=2.[Li:20]CCCC>CCCCC>[CH3:1][C:2]1[CH-:3][C:4]2[C:9]([CH:10]=1)=[C:8]([C:11]1[CH:12]=[C:13]([CH3:18])[CH:14]=[C:15]([CH3:17])[CH:16]=1)[C:7]([CH3:19])=[CH:6][CH:5]=2.[Li+:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 231153062,5-Dimethyl-4-(3,5-dimethylphenyl)indene2회HCID 178418339Butyllithium

생성물 1

HCID 23708019Lithium[2,5-dimethyl-4-(3,5-dimethylphenyl)indenide]

시약·촉매·용매 1

HCID 8003Pentane용매

실험 절차

2,5-Dimethyl-4-(3,5-dimethylphenyl)indene (2.1 g, 8.4 mmol), prepared as described under (f) above, was dissolved in 60 ml of pentane. To this solution was added 3.4 ml of nBuLi (2.5 M in hexane) and the reaction was stirred for two hours at room temperature. A white solid precipitated from solution and was collected by frit filtration and washed with additional pentane. Yield: 1.6 g (74%).

후처리

  1. customA white solid precipitated from solution
  2. filtrationwas collected by frit filtration
  3. washwashed with additional pentane

출처 및 근거

ORD 기록
ord-c30dc50639ca426b9378ae7fbe2a2384
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157591B2

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