Dimethylformamide → 4-Chloro-3-methylbenzoyl chloride

HRID 500945

反応式

HRID 500945 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[CH3:11].CN(C=O)C.C(Cl)(=O)C([Cl:20])=O>C(Cl)Cl>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([Cl:20])=[O:7])=[CH:4][C:3]=1[CH3:11]

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 2829894-Chloro-3-methylbenzoic acid

生成物 1

HCID 130583754-Chloro-3-methylbenzoyl chloride

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a suspension of 52.55 g (0.31 mol) of 4-chloro-3-methyl-benzoic acid in CH2Cl2 (1.2 L) with DMF (1 mL) at 0° C. under N2 with an outlet sparging through 2.5 N sodium hydroxide was added 29.56 mL (0.339 mol) of oxalyl chloride. The mixture was allowed to warm to room temperature over a 3 h period. The reaction mixture was concentrated and taken forward crude.

後処理

  1. customsparging through 2.5 N sodium hydroxide
  2. concentrationThe reaction mixture was concentrated

出典と根拠

ORDレコード
ord-98621b18a7b345418321c9ad9af11e41
出典データセット
uspto-grants-2010_08
特許番号
US07772236B2

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