Indene → HCID 178484298、化合物

HRID 1033868ノート

反応式

HRID 1033868 の反応式
[CH3:1][N-:2][CH3:3].[CH3:4][N-:5][CH3:6].[CH3:7][N-:8][CH3:9].C[N-]C.[Ti+4:13].[CH2:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15]1>C1(C)C=CC=CC=1>[CH3:1][N-:2][CH3:3].[CH3:4][N-:5][CH3:6].[CH3:7][N-:8][CH3:9].[CH:14]1([Ti+3:13])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15]1

参加物

4

反応物 2

HCID 7219IndeneHCID 123185Methanamine, N-methyl-, titanium(4+) salt (4:1)

生成物 1

HCID 178484298HCID 178484298、化合物収率 70%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A 250 mL Schlenk flask is charged with toluene, 75 mL, and titanium tetrakis(dimethylamide), 2.35 g (10.48 mmole). The mixture is stirred magnetically throughout the procedure. Freshly degassed indene (nitrogen sparged) is added to the Schlenk flask at room temperature in excess, 2.44 mL (20.96 mmole). The mixture is refluxed at least 24 hours giving a blood red solution. All volatiles are removed under vacuum at room temperature leaving a deep red, oily residue. The residue is transferred in a minimum of hexane to a micro scale distillation apparatus and distilled under vacuum. A viscous red oil distills at 60° C. (0.025 mm Hg) which is identified by nuclear magnetic resonance (NMR) as indenyltitanium tris(dimethylamide). The yield is 70% by this method of preparation.

後処理

  1. temperatureThe mixture is refluxed at least 24 hours
  2. customgiving a blood red solution
  3. customAll volatiles are removed under vacuum at room temperature
  4. customleaving a deep red, oily residue
  5. distillationThe residue is transferred in a minimum of hexane to a micro scale distillation apparatus
  6. distillationdistilled under vacuum
  7. distillationA viscous red oil distills at 60° C. (0.025 mm Hg) which
  8. customThe yield is 70% by this method of preparation

出典と根拠

ORDレコード
ord-ebaf1ac337b3424d8eb584f997b45e76
出典データセット
uspto-grants-1994_05
特許番号
US05312938

反応ノート

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