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Water → Disiloxane, 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyl-

HRID 1248743
ノート
印刷プレビュー

反応式

HRID 1248743 の反応式
[Cl:1][CH2:2][CH2:3][CH2:4][Si:5](Cl)([CH3:7])[CH3:6].C(=O)([O-])[O-].[Na+].[Na+].[OH2:15]>>[Cl:1][CH2:2][CH2:3][CH2:4][Si:5]([CH3:7])([CH3:6])[O:15][Si:5]([CH2:4][CH2:3][CH2:2][Cl:1])([CH3:7])[CH3:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 962WaterHCID 10340Sodium CarbonateHCID 82765Silane, chloro(3-chloropropyl)dimethyl-2 回

生成物 1

HCID 87463Disiloxane, 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyl-収率 89%

実験手順

To a triangular flask of 2 l containing 1200 ml of water was added dropwise 342 g of 3-chloropropylchlorodimethylsilane (hereinafter referred to as "CPCDMSi") in an hour while stirring with a magnetic stirrer at a room temperature. After completion of the addition, the reaction mixture was neutralized with sodium carbonate and then extracted three times with each 500 ml of n-hexane. After drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane was removed under reduced pressure. The obtained residue was distilled under reduced pressure, and then the distillate obtained at 103° C./1.5 mmHg was collected to give 255 g (Yield 89%) of 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyldisiloxane (hereinafter referred to as "BCPSi").

後処理

  1. customin an hour
  2. additionAfter completion of the addition
  3. extractionextracted three times with each 500 ml of n-hexane
  4. dry with materialAfter drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane
  5. customwas removed under reduced pressure
  6. distillationThe obtained residue was distilled under reduced pressure
  7. customthe distillate obtained at 103° C./1.5 mmHg
  8. customwas collected

出典と根拠

ORDレコード
ord-183c214edbe94ae8a1b2f00cd9c726de
出典データセット
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04525563

反応ノート

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