Potassium bis(trimethylsilyl)amide → HCID 23684418、化合物

HRID 1595106ノート

反応式

HRID 1595106 の反応式
[CH3:1][C:2]1[CH2:3][C:4]2[C:9]([CH:10]=1)=[C:8](C1C3C(=CC=CC=3)C=CC=1)[CH:7]=[CH:6][CH:5]=2.C[Si]([N-][Si](C)(C)C)(C)C.[K+:30]>C1(C)C=CC=CC=1>[CH3:10][C:2]1[CH:1]=[C:10]([C:2]2[CH-:3][C:4]3[C:9]([CH:1]=2)=[CH:8][CH:7]=[CH:6][CH:5]=3)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[K+:30]

参加物

4

反応物 2

HCID 3251421Potassium bis(trimethylsilyl)amideHCID 177791321-(2-Methyl-1H-inden-4-yl)naphthalene

生成物 1

HCID 23684418HCID 23684418、化合物収率 228.5%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

2-Methyl-4-naphthylindene (1.00 g, 3.27 mmole) was dissolved in 20 ml of toluene, potassium bis(trimethylsilyl)amide (1.05 equivalent, 3.43 mmole, 0.684 g) was added and the reaction mixture was stirred at room temperature for 24 hours, during which a yellow solid precipitated. Hexane was added (20 ml) and the mixture was stirred for 2 h. The solid product was isolated by vacuum filtration through a medium porosity frit. The solid was pumped dry giving 1.10 g, 98 percent of the desired product.

後処理

  1. customprecipitated
  2. additionHexane was added (20 ml)
  3. stirringthe mixture was stirred for 2 h
  4. customThe solid product was isolated by vacuum filtration through a medium porosity frit
  5. customThe solid was pumped dry

出典と根拠

ORDレコード
ord-487154d8dff5413a8ac1f89d001577a3
出典データセット
uspto-grants-2001_09
特許番号
US06284905B1

反応ノート

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