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Water → HCID 12804956、化合物

HRID 224222
ノート
印刷プレビュー

反応式

HRID 224222 の反応式
[Cl:1][C:2]1[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:3]=1[O:4][C:5]1[CH:15]=[CH:14][C:8]([O:9][CH:10]([CH3:13])[CH2:11]O)=[CH:7][CH:6]=1.N1C=CC=CC=1.S(Cl)([Cl:29])=O.O>C(OCC)C>[Cl:1][C:2]1[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:3]=1[O:4][C:5]1[CH:15]=[CH:14][C:8]([O:9][CH:10]([CH3:13])[CH2:11][Cl:29])=[CH:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1049PyridineHCID 24386Thionyl ChlorideHCID 12804883HCID 12804883、化合物

生成物 1

HCID 12804956HCID 12804956、化合物収率 78.7%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

3.0 g of β-[4-(2,4-Dichlorophenoxy)phenoxy]propanol and 1.1 g of pyridine were dissolved in 50 ml of anhydrous diethyl ether, and 1.5 g of thionyl chloride was added dropwise to the solution while cooling. The mixture was then heated for 1 hour while refluxing. The reaction mixture was poured into an appropriate amount of water, and the mixture was extracted with diethyl ether. The extract was washed with water and dried over anhydrous sodium sulfate. The ether was removed by distillation and the residue was distilled under reduced pressure to obtain 2.5 g of the desired product having a boiling point of 192° to 194° C./2 mmHg.

後処理

  1. temperaturewhile cooling
  2. temperatureThe mixture was then heated for 1 hour
  3. temperaturewhile refluxing
  4. extractionthe mixture was extracted with diethyl ether
  5. washThe extract was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe ether was removed by distillation
  8. distillationthe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-983defbd0fa54814abd48cc954db4955
出典データセット
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04231787

反応ノート

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