1,2-Dibromoethane → 6-(2-Bromoethoxy)salicylamide

HRID 615228

反応式

HRID 615228 の反応式
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[C:3]=1[C:4]([NH2:6])=[O:5].C(=O)([O-])[O-].[K+].[K+].[Br:18][CH2:19][CH2:20]Br>C(#N)C>[Br:18][CH2:19][CH2:20][O:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[C:3]=1[C:4]([NH2:6])=[O:5]

参加物

5

反応物 3

HCID 78391,2-DibromoethaneHCID 11430Potassium CarbonateHCID 766022,6-Dihydroxybenzamide

生成物 1

HCID 137544236-(2-Bromoethoxy)salicylamide

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained.

後処理

  1. temperatureis refluxed
  2. filtrationThe reaction mixture is filtered
  3. temperaturewhilst still warm
  4. concentrationthe filtrate concentrated by evaporation
  5. customthe residue recrystallised from a little methanol

出典と根拠

ORDレコード
ord-47163b8fb6ae49a9b4394f743130485c
出典データセット
uspto-grants-1985_02
特許番号
US04497813

関連ノート

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