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Pyridine → 2-chloro-N-(3-chloro-4-fluorophenyl)acetamide

HRID 4469
ノート
印刷プレビュー

反応式

HRID 4469 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[F:9])[NH2:5].N1C=CC=CC=1.[Cl:16][CH2:17][C:18](Cl)=[O:19]>C1(C)C=CC=CC=1>[Cl:16][CH2:17][C:18]([NH:5][C:4]1[CH:6]=[CH:7][C:8]([F:9])=[C:2]([Cl:1])[CH:3]=1)=[O:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1049PyridineHCID 6577Chloroacetyl chlorideHCID 97083-Chloro-4-fluoroaniline

生成物 1

HCID 7358492-chloro-N-(3-chloro-4-fluorophenyl)acetamide収率 88%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To 130 ml. of toluene was added, with stirring, 24.0 g. (0.165 mole) of 3-chloro-4-fluoroaniline and 13.5 ml. (0.166 mole) of pyridine. The resulting solution was cooled to ca 0° C. and 13.2 ml. (0.166 mole) of 2-chloroacetyl chloride was added. The reaction mixture was stirred at room temperature for 5 hours and then it was extracted twice with 100 ml. of 1N hydrochloric acid, followed by 100 ml. of saturated sodium chloride solution. The resulting toluene solution was dried using magnesium sulfate, and then it was concentrated in vacuo to give 32.6 g. (88% yield) of N-(2-chloroacetyl)-3-chloro-4-fluoroaniline.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureThe resulting solution was cooled to ca 0° C.
  2. stirringThe reaction mixture was stirred at room temperature for 5 hours
  3. extractionit was extracted twice with 100 ml
  4. dry with materialThe resulting toluene solution was dried
  5. concentrationit was concentrated in vacuo
  6. customto give 32.6 g

出典と根拠

ORDレコード
ord-67d46a104ad240b9a00c308bf07eb4cb
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04725616

反応ノート

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