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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Lithium → 2,2'-Phosphanediyldipyridine

HRID 1048825
ノート
印刷プレビュー

反応式

HRID 1048825 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 129784732,2'-Phosphanediyldipyridine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-378f7ae349a4443988c989b97b9603e2
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09381503B2

反応ノート

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