Thionyl Chloride → 3-methoxy-4-nitro-benzoyl Chloride

HRID 55251

反応式

HRID 55251 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13])[C:6](O)=[O:7].S(Cl)([Cl:17])=O>C(CC(C)(C)C)(C)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13])[C:6]([Cl:17])=[O:7]

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 787643-Methoxy-4-nitrobenzoic acid

生成物 1

HCID 111276553-methoxy-4-nitro-benzoyl Chloride

試薬・触媒・溶媒 1

HCID 109072,2,4-Trimethylpentane溶媒

実験手順

A stirred suspension of 1.0 g of 3-methoxy-4-nitrobenzoic acid and 1.40 ml of thionyl chloride is heated to reflux for 2 hours. The mixture is cooled to room temperature, 2 ml of iso-octane added and the mixture evaporated in vacuo to a solid residue. The residue is washed with iso-octane (2×2 ml), dried in vacuo to give 1.08 g of cream colored solid.

後処理

  1. temperatureis heated
  2. temperatureto reflux for 2 hours
  3. customthe mixture evaporated in vacuo to a solid residue
  4. washThe residue is washed with iso-octane (2×2 ml)
  5. customdried in vacuo
  6. customto give 1.08 g of cream

出典と根拠

ORDレコード
ord-7bbacb0f150a4f3597ed06de4962c7f0
出典データセット
uspto-grants-1997_04
特許番号
US05624923

関連ノート

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