ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

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

HRID 11972
ノート
印刷プレビュー

反応式

HRID 11972 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7ded912e93ad40fc8c34118387fd0250
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07098356B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート