Triethylamine → HCID 178439034、化合物

HRID 16052ノート

反応式

HRID 16052 の反応式
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[N:13]1[CH2:17][C:16](=[NH:18])[N:15]([C:19]2[C:24]([CH:25]([CH3:27])[CH3:26])=[CH:23][CH:22]=[CH:21][C:20]=2[CH:28]([CH3:30])[CH3:29])[CH2:14]1)([CH3:3])[CH3:2].[Cl-:31].[Cl-].[Cl-].[CH:34]1([Ti+3:39])[CH:38]=[CH:37][CH:36]=[CH:35]1.C(N(CC)CC)C>C1(C)C=CC=CC=1>[Cl-:31].[Cl-:31].[CH:34]1([Ti+2:39])[CH:38]=[CH:37][CH:36]=[CH:35]1.[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[N:13]1[CH2:17][C:16](=[NH:18])[N:15]([C:19]2[C:20]([CH:28]([CH3:30])[CH3:29])=[CH:21][CH:22]=[CH:23][C:24]=2[CH:25]([CH3:27])[CH3:26])[CH2:14]1)([CH3:3])[CH3:2]

参加物

5

反応条件

温度
4 °C

実験手順

To a suspension of 1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline (2.03 g, 5.0 mmol) and cyclopentadienyltitanium trichloride (1.10 g, 5.0 mmol) in toluene (30 mL) was added triethylamine (0.8 mL, 5.7 mmol) at ambient temperature. After stirring for 1 hour, the thick yellow-orange suspension was diluted with toluene (50 mL) and ligroin (120 mL). The suspension was heated to reflux and filtered hot. Cooling to approx. 4° C. afforded yellow crystals, which were filtered and washed with cold ligroin to give 1.34 g (46% yield) of NMR pure 1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline cyclopentadienyl titanium dichloride.

後処理

  1. temperatureThe suspension was heated
  2. temperatureto reflux
  3. filtrationfiltered hot
  4. customafforded yellow crystals, which
  5. filtrationwere filtered
  6. washwashed with cold ligroin

出典と根拠

ORDレコード
ord-b1afdfd9f1f9444687c2d4ea9363ccca
出典データセット
uspto-grants-2010_06
特許番号
US07737070B2

反応ノート

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