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Thionyl Chloride → 4-Chloro-2-methoxybenzoyl chloride

HRID 78478
ノート
印刷プレビュー

反応式

HRID 78478 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1.O=S(Cl)[Cl:15]>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([Cl:15])=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24386Thionyl ChlorideHCID 936824-Chloro-o-anisic acid

生成物 1

HCID 221424504-Chloro-2-methoxybenzoyl chloride

実験手順

A solution of the 4-chloro-2-methoxybenzoic acid (0.24 g, 1.3 mmol) in 7 mL of SOCl2 was warmed to reflux and was allowed to stir for 2 hours. The mixture was cooled to ambient temperature and concentrated under reduced pressure. The crude material was diluted with 5 mL of toluene and concentrated under reduced pressure. This dilution with toluene and concentration was repeated two additional times to give the crude title compound which was used without additional purification or characterization.

後処理

  1. temperatureto reflux
  2. concentrationconcentrated under reduced pressure
  3. additionThe crude material was diluted with 5 mL of toluene
  4. concentrationconcentrated under reduced pressure
  5. concentrationThis dilution with toluene and concentration

出典と根拠

ORDレコード
ord-6301097ee8fe426b99de7fb20b919ba6
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08841334B2

反応ノート

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