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Lithium → 2,2'-Phosphanediyldipyridine

HRID 1048825
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HRID 1048825 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[P:7](C1C=CC=CN=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1.[Li]>C1COCC1>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[PH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1
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참가 물질

4

반응물 2

HCID 3028194LithiumHCID 11065346Pyridine, 2,2',2''-phosphinidynetris-

생성물 1

HCID 129784732,2'-Phosphanediyldipyridine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The tris(pyridin-2-yl)phosphine (22.4 g, 85 mmol) was suspended in THF (400 ml). To this were added lithium granules (5.0 g, 720 mmol). The mixture was then stirred at room temperature for four hours. This gave an intense red solution. The solution was then filtered into a clean Schlenk flask to remove any un-reacted lithium metal. The solvent was then removed under vacuum and water (100 ml, degassed with nitrogen gas for 20 minutes) added. Ether (400 ml) was then added and the biphasic solution stirred for 20 minutes. The upper (organic) phase was then cannula transferred into a clean Schlenk flask and then dried under vacuum. This gave dark orange/red oil. Yield=15.1 g, 94% 31P{1H}NMR (121 MHz, CDCl3) ä; −33.8 (s, PPy2).

후처리

  1. customThis gave an intense red solution
  2. filtrationThe solution was then filtered into a clean Schlenk flask
  3. customto remove any un-reacted lithium metal
  4. customThe solvent was then removed under vacuum and water (100 ml, degassed with nitrogen gas for 20 minutes)
  5. additionadded
  6. additionEther (400 ml) was then added
  7. stirringthe biphasic solution stirred for 20 minutes
  8. customcannula transferred into a clean Schlenk flask
  9. customdried under vacuum

출처 및 근거

ORD 기록
ord-378f7ae349a4443988c989b97b9603e2
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09381503B2

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