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1-Octanol → HCID 608399、化合物

HRID 1901259
ノート
印刷プレビュー

反応式

HRID 1901259 の反応式
[CH2:1]([OH:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].N1C=CC=CC=1.[CH3:16][CH:17]([SiH:19]([CH:21]([CH3:23])[CH3:22])Cl)[CH3:18]>CCCCCC>[CH3:16][CH:17]([SiH:19]([CH:21]([CH3:23])[CH3:22])[O:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH3:18]
参加物反応条件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 9571-OctanolHCID 1049PyridineHCID 2758383Chlorodi(isopropyl)silane

生成物 1

HCID 608399HCID 608399、化合物

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

反応条件

温度
-5 °C

実験手順

Di(2-propyl)octyloxysilane was prepared in the following manner. Dry octanol (52.5 g, 0.40 mole) and dry pyridine (32.9 g, 0.42 mole) were added to a 500 ml round-bottom flask. The solution was cooled to -5° C. with stirring. Di(2-propyl)chlorosilane (67.1 g, 0.44 mole) was added in a dropwise fashion over 60 minutes. After this addition, the temperature of the reaction mixture was maintained at -5° C. for another 30 minutes, then allowed to come to room temperature overnight. Hexane (100 ml) was then added to this reaction mixture. The organic phase was extracted with 500 ml 0.1N aq. HCl and 500 ml water. The organic layer was dried over anhydrous magnesium sulfate, filtered and distilled to produce di(2-propyl)octyloxysilane.

後処理

  1. customDi(2-propyl)octyloxysilane was prepared in the following manner
  2. additionAfter this addition
  3. temperaturethe temperature of the reaction mixture was maintained at -5° C. for another 30 minutes
  4. extractionThe organic phase was extracted with 500 ml 0.1N aq. HCl and 500 ml water
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. distillationdistilled

出典と根拠

ORDレコード
ord-a7c0143c6afd4d43bd7bbcd6b3bdbf43
出典データセット
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05576453

反応ノート

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