Dimethylformamide → 4-Cyano-2-methoxybenzoyl chloride

HRID 1352651ノート

反応式

HRID 1352651 の反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([C:12]#[N:13])[CH:9]=[CH:8][C:4]=1[C:5](O)=[O:6].C(Cl)(=O)C([Cl:17])=O.CN(C=O)C>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([C:12]#[N:13])[CH:9]=[CH:8][C:4]=1[C:5]([Cl:17])=[O:6]

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 151660044-Cyano-2-methoxybenzoic acid

生成物 1

HCID 226750494-Cyano-2-methoxybenzoyl chloride収率 100%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

2-Methoxy-4-cyanobenzoic acid (Tetrahedron Letters, 1986, 27(49), 5997–6000) (1 g, 5.6 mmol) was dissolved in CH2Cl2 (20 ml). Oxalyl chloride (1.5 ml, 8.2 mmol) was rapidly introduced into the solution and a drop of DMF was added. A vigorous reaction took place with the abundant evolution of gaseous products. The solution was stirred for 1 h then allowed to stand over night. Solvent was removed using a rotary evaporator to leave 1.1 g of an off white solid (5.6 mmol, yield 99%) that was used without further purification.

後処理

  1. customA vigorous reaction
  2. waitto stand over night
  3. customSolvent was removed
  4. customa rotary evaporator

出典と根拠

ORDレコード
ord-7403f8314eb443eabef2280ee38c83b1
出典データセット
uspto-grants-2007_05
特許番号
US07220769B2

反応ノート

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