Thionyl Chloride → 2-(2-Chloroethoxy)-1,3-dimethoxybenzene

HRID 868506ノート

反応式

HRID 868506 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[C:4]=1[O:5][CH:6](O)[CH3:7].S(Cl)([Cl:17])=O>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[C:4]=1[O:5][CH2:6][CH2:7][Cl:17]

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 14886366HCID 14886366、化合物

生成物 1

HCID 133059082-(2-Chloroethoxy)-1,3-dimethoxybenzene

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A solution of 7.77 g of 2,6-dimethoxyphenoxyethanol in 30 ml of pyridine was cooled and 4.7 g of thionylchloride was added with stirring. After 20 minutes, stirring, the reaction mixture was heated on the steam bath for 2 hours. After cooling, the reaction mixture was evaporated in reduced pressure. The residue was extracted with CHCl3, purified with silicagel chromatography (eluent: EtOAc) 1.82 g of objective compound was obtained.

後処理

  1. stirringstirring
  2. temperaturethe reaction mixture was heated on the steam bath for 2 hours
  3. temperatureAfter cooling
  4. customthe reaction mixture was evaporated in reduced pressure
  5. extractionThe residue was extracted with CHCl3
  6. custompurified with silicagel chromatography (eluent: EtOAc) 1.82 g of objective compound
  7. customwas obtained

出典と根拠

ORDレコード
ord-607a922964134f7aa0ee55f90dc64397
出典データセット
uspto-grants-1988_10
特許番号
US04780462

反応ノート

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