Water → 3-Carbomethoxy-4-[(chloroacetyl)amino]thiophene

HRID 67382

反応式

HRID 67382 の反応式
Cl.[C:2]([C:6]1[C:10]([NH2:11])=[CH:9][S:8][CH:7]=1)([O:4][CH3:5])=[O:3].[Cl:12][CH2:13][C:14](Cl)=[O:15].C(N(CC)CC)C.O>C(Cl)Cl>[C:2]([C:6]1[C:10]([NH:11][C:14](=[O:15])[CH2:13][Cl:12])=[CH:9][S:8][CH:7]=1)([O:4][CH3:5])=[O:3]

参加物

6

反応物 4

HCID 962WaterHCID 6577Chloroacetyl chlorideHCID 8471TriethylamineHCID 2777609Methyl 4-aminothiophene-3-carboxylate Hydrochloride

生成物 1

HCID 145100033-Carbomethoxy-4-[(chloroacetyl)amino]thiophene

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A suspension of 12.2 g (0.063 mol) of 3-carbomethoxy-4-aminothiophene hydrochloride in 100 ml of methylene chloride is treated with 10 ml (0.126 mol) of chloroacetyl chloride and subsequently dropwise with 17.6 ml (0.126 mol) of triethylamine, the temperature being held below 25° C. The solution is poured into water and extracted twice with 50 ml of methylene chloride each time. The combined methylene chloride extracts are washed three times with 50 ml of water each time, dried over magnesium sulphate and evaporated. After chromatography on silica gel using methylene chloride for the elution, there is obtained crystalline 3-carbomethoxy-4-[(chloroacetyl)amino]thiophene of melting point 98°-100° C.

後処理

  1. custombeing held below 25° C
  2. extractionextracted twice with 50 ml of methylene chloride each time
  3. washThe combined methylene chloride extracts are washed three times with 50 ml of water each time
  4. dry with materialdried over magnesium sulphate
  5. customevaporated
  6. washfor the elution

出典と根拠

ORDレコード
ord-fbe620667c7a404fb4944d05931487c8
出典データセット
uspto-grants-1982_08
特許番号
US04346031

関連ノート

読み込み中…