Triethoxysilane → Phenethyltriethoxysilane

HRID 843305

反応式

HRID 843305 の反応式
[CH2:1]([O:3][SiH:4]([O:8][CH2:9][CH3:10])[O:5][CH2:6][CH3:7])[CH3:2].CC1C=C(N([C:28]2[CH:35]=[CH:34][C:31]([CH:32]=[CH2:33])=[CH:30][CH:29]=2)C2C=CC(C)=C(C)C=2)C=CC=1C>C1(C)C=CC=CC=1>[CH2:1]([O:3][Si:4]([O:8][CH2:9][CH3:10])([O:5][CH2:6][CH3:7])[CH2:33][CH2:32][C:31]1[CH:34]=[CH:35][CH:28]=[CH:29][CH:30]=1)[CH3:2]

参加物

4

反応物 2

HCID 13830TriethoxysilaneHCID 108927834-[N,N-bis(3,4-dimethylphenyl)amino]styrene

生成物 1

HCID 11097560Phenethyltriethoxysilane収率 94.2%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

Into a three-necked flask, 40 ml of toluene, 6.0 g (37 mmol) of triethoxysilane and 0.34 mmol of platinum (II) dichloro(h-cycloocta-1,5-diene) were placed, and 20 ml of a toluene solution containing 9.9 g of 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene was added dropwise with stirring at room temperature. After the addition was completed, the mixture was stirred at 70° C. for 3 hours, and thereafter the solvent was removed under reduced pressure to obtain oily pale yellow 4-[N,N-bis(3,4-dimethylphenyl)amino]-[2-(triethoxysilyl)ethylbenzene in an amount of 14.0 g (yield: 94.2%).

後処理

  1. additionwas added dropwise
  2. additionAfter the addition
  3. stirringthe mixture was stirred at 70° C. for 3 hours
  4. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-fac7e20dbc594c7189953ca6f2fc07cb
出典データセット
uspto-grants-2002_04
特許番号
US06376695B1

関連ノート

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