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Dimethylcarbamoyl Chloride → 3,5-Dibromopicolinonitrile

HRID 1352766
ノート
印刷プレビュー

反応式

HRID 1352766 の反応式
[Br:1][C:2]1[CH:3]=[N+:4]([O-])[CH:5]=[C:6]([Br:8])[CH:7]=1.C[Si]([C:14]#[N:15])(C)C.CN(C)C(Cl)=O.C(=O)([O-])O.[Na+]>C(Cl)Cl>[C:14]([C:3]1[C:2]([Br:1])=[CH:7][C:6]([Br:8])=[CH:5][N:4]=1)#[N:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6598Dimethylcarbamoyl Chloride2 回HCID 82115Trimethylsilyl cyanide2 回HCID 516892Sodium BicarbonateHCID 6200033,5-Dibromopyridine N-oxide

生成物 1

HCID 123612023,5-Dibromopicolinonitrile

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A mixture of 3,5-dibromopyridine N-oxide (prepared in the above (1)) 2.26 g, trimethylsilylcyanide 1.06 g and dimethylcarbamic acid chloride 1.15 g in methylene chloride 25 ml is refluxed under heating for 1 day. To the mixture are added trimethylsilylcyanide 443 mg and dimethylcarbamic acid chloride 480 mg, and the mixture is refluxed under heating for 20 hours. An aqueous sodium hydrogen carbonate solution is added to the reaction mixture cooled, and the mixture is extracted with methylene chloride. The combined extract is washed, dried and the solvent is removed in vacuo. The residue is purified by silica gel chromatography (solvent; n-hexane:ethyl acetate=1:1) to give 2-cyano-3,5-dibromopyridine 1.38 g. mp 109–112° C.

後処理

  1. temperatureis refluxed
  2. temperatureunder heating for 1 day
  3. temperaturethe mixture is refluxed
  4. temperatureunder heating for 20 hours
  5. temperaturecooled
  6. extractionthe mixture is extracted with methylene chloride
  7. extractionThe combined extract
  8. washis washed
  9. customdried
  10. customthe solvent is removed in vacuo
  11. customThe residue is purified by silica gel chromatography (solvent; n-hexane:ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-df90a6878b634bb2a9f7b39a50c7460e
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07220736B2

反応ノート

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