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2-Neopentylindene → (2-neopentylinden-1-yl)-N-(1,1-dimethylethyl)dimethylsilanamine

HRID 11972
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HRID 11972 반응식
[CH2:1]([C:6]1[CH2:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:2]([CH3:5])([CH3:4])[CH3:3].C([Li])CCC.[Cl-].[CH3:21][C:22]([NH:25][SiH:26]([CH3:28])[CH3:27])([CH3:24])[CH3:23]>C1COCC1>[CH2:1]([C:6]1[CH:14]([Si:26]([CH3:28])([CH3:27])[NH:25][C:22]([CH3:24])([CH3:23])[CH3:21])[C:13]2[C:8]([CH:7]=1)=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:2]([CH3:5])([CH3:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 219770112-NeopentylindeneHCID 131725908N-(1,1-dimethylethyl)dimethylsilanamine chlorideHCID 178418339Butyllithium

생성물 1

HCID 69306382(2-neopentylinden-1-yl)-N-(1,1-dimethylethyl)dimethylsilanamine수율 103.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a mixture of 2-neopentylindene (0.81 g, 4.3 mmol) in 30 mL of hexanes were added 2.9 mL of butyl lithium (1.6 M hexane; 4.7 mmol). The mixture was stirred for one hour, diluted with 20 mL of THF and to this added N-(1,1-dimethylethyl)dimethylsilanamine chloride (1.84 g, 11.2 mmol) in 10 mL of THF. After stirring overnight, the volatiles were removed in vacuo, the residue extracted with hexane, filtered and the volatiles removed in vacuo to give 1.4 g (102 percent) of a yellow oil.

후처리

  1. stirringAfter stirring overnight
  2. customthe volatiles were removed in vacuo
  3. extractionthe residue extracted with hexane
  4. filtrationfiltered
  5. customthe volatiles removed in vacuo

출처 및 근거

ORD 기록
ord-7ded912e93ad40fc8c34118387fd0250
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07098356B2

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