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Thionyl Chloride → HCID 20485210、化合物

HRID 647549
ノート
印刷プレビュー

反応式

HRID 647549 の反応式
[Cl:1][C:2]([Cl:11])=[CH:3][CH:4]([CH:8]([CH3:10])[CH3:9])[C:5](O)=[O:6].S(Cl)([Cl:14])=O>C1C=CC=CC=1>[Cl:1][C:2]([Cl:11])=[CH:3][CH:4]([CH:8]([CH3:10])[CH3:9])[C:5]([Cl:14])=[O: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 2

HCID 24386Thionyl ChlorideHCID 13246126alpha-(2,2-Dichlorovinyl)isovaleric acid

生成物 1

HCID 20485210HCID 20485210、化合物

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

In 20 ml of dry benzene were dissolved 2.0 g of α-(2,2-dichlorovinyl)isovaleric acid, followed by the addition of 6.0 g of thionyl chloride. The mixture was refluxed overnight. It was then distilled to remove the low-boiling fraction, whereby α-(2,2-dichlorovinyl)isovaleroyl chloride was obtained. This α-(2,2-dichlorovinyl)isovaleroyl chloride was dissolved in 25 ml of dry benzene, followed by the addition of 2.3 g of α-cyano-3-phenoxybenzyl alcohol and, then, 2.4 g of pyridine. The mixture was stirred at room temperature overnight. The resultant reaction mixture was diluted with diethyl ether, washed with water and dilute aqueous hydrogen chloride, dried over anhydrous magnesium sulfate and distilled to remove the low-boiling fraction. Column chromatography was carried out on the residue to obtain 3.2 g of α-cyano-3-phenoxybenzyl α-(2,2-dichlorovinyl)isovalerate (Compound [1]) which was shown to have the properties given below [yield: 78% based on α-(2,2-dichlorovinyl)isovaleric acid].

後処理

  1. temperatureThe mixture was refluxed overnight
  2. distillationIt was then distilled
  3. customto remove the low-boiling fraction

出典と根拠

ORDレコード
ord-f37e0de499be4e09a2b7b9327fa58ae1
出典データセット
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04409238

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