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Water → HCID 11076628、化合物

HRID 1792313
ノート
印刷プレビュー

反応式

HRID 1792313 の反応式
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:7][OH:8].[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.O>N1C=CC=CC=1>[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15]([O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][O:2][CH3:1])(=[O:17])=[O:16])=[CH:11][CH:10]=1
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 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 8134Diethylene Glycol Monomethyl Ether

生成物 1

HCID 11076628HCID 11076628、化合物収率 98.4%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a solution of diethylene glycol monomethylether (12 g, 100 mmol) in pyridine (70 ml) was added p-toluenesulfonyl chloride (22.8 g, 120 mmol) at 0° C., which was then stirred at room temperature for 2 hours. Water was added thereto, and the mixture was extracted with diethyl ether. The extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution, and dried over anhydrous magnesium sulfate. The organic solvent was removed under reduced pressure to give the title compound (27 g, stoichiometric yield) as a yellow oil. The compound thus obtained was used in the next reaction without further purification.

後処理

  1. extractionthe mixture was extracted with diethyl ether
  2. washThe extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe organic solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-8c8a90937fc941d6aa4e1f527bfdf07d
出典データセット
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07074819B2

反応ノート

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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