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Methanol → HCID 54364994、化合物

HRID 1646466
ノート
印刷プレビュー

反応式

HRID 1646466 の反応式
[NH2:1][C:2]1[C:3]([F:16])=[CH:4][C:5]([Cl:15])=[C:6]([S:8][C:9]2([C:12]([OH:14])=[O:13])[CH2:11][CH2:10]2)[CH:7]=1.[CH3:17]O>S(=O)(=O)(O)O>[CH3:17][O:13][C:12]([C:9]1([S:8][C:6]2[CH:7]=[C:2]([NH2:1])[C:3]([F:16])=[CH:4][C:5]=2[Cl:15])[CH2:11][CH2:10]1)=[O:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 887MethanolHCID 198006261-(5-Amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid

生成物 1

HCID 54364994HCID 54364994、化合物

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid触媒

実験手順

A solution of 3.6 g of 1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid and a few drops of sulfuric acid in 50 ml of methanol is heated under reflux until the starting material can no longer be detected. The methanol is then evaporated off, water and ethyl acetate are added to the residue and the organic phase is washed in succession with sodium hydrogen carbonate solution, water and saturated sodium chloride solution. Concentration and purification of the crude product by means of silica gel chromatography yield 5.7 g of 1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid methyl ester having a melting point of from +119° to +121° C.

後処理

  1. temperatureunder reflux until the starting material
  2. customThe methanol is then evaporated off
  3. additionwater and ethyl acetate are added to the residue
  4. washthe organic phase is washed in succession with sodium hydrogen carbonate solution, water and saturated sodium chloride solution
  5. concentrationConcentration and purification of the crude product by means of silica gel chromatography yield 5.7 g of 1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid methyl ester having a melting point of from +119° to +121° C.

出典と根拠

ORDレコード
ord-e62f18c31d874f4b8141c63cea525f38
出典データセット
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05180418

反応ノート

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