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Chloroform → Ethyl 2,6-difluorobenzene-1-carboximidate

HRID 2050197
ノート
印刷プレビュー

反応式

HRID 2050197 の反応式
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4]([NH2:6])=[O:5].[B-](F)(F)(F)F.[CH3:17][CH2:18][O+](CC)CC.C(Cl)(Cl)Cl>C(Cl)Cl>[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4](=[NH:6])[O:5][CH2:17][CH3:18]
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 6212ChloroformHCID 874392,6-DifluorobenzamideHCID 2723982Triethyloxonium tetrafluoroborate

生成物 1

HCID 13730259Ethyl 2,6-difluorobenzene-1-carboximidate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

2,6-Difluorobenzamide (1.56 g) in methylene chloride was added to triethyloxonium fluoborate (1.9 g) in methylene chloride and the mixture stirred for 24 hours. The solution was then washed three times with cold sodium carbonate solution and dried over sodium sulphate. The methylene chloride solution was evaporated to yield an oil. This was mixed with chloroform and the solution filtered from insoluble material. Evaporation of the chloroform gave the ethyl 2,6-difluorobenzimidate as a mobile oil.

後処理

  1. washThe solution was then washed three times with cold sodium carbonate solution
  2. dry with materialdried over sodium sulphate
  3. customThe methylene chloride solution was evaporated
  4. customto yield an oil
  5. filtrationthe solution filtered from insoluble material
  6. customEvaporation of the chloroform

出典と根拠

ORDレコード
ord-72431eb1f88f400994e63823c8b9c124
出典データセット
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04200653

反応ノート

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