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Phosphorus oxychloride → 8-Bromo-4-chloroquinoline

HRID 1403095
ノート
印刷プレビュー

反応式

HRID 1403095 の反応式
P(Cl)(Cl)([Cl:3])=O.[Br:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[NH:15][CH:14]=[CH:13][C:12]2=O>>[Br:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[N:15]=[CH:14][CH:13]=[C:12]2[Cl:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 124036828-Bromo-1,4-dihydroquinolin-4-one

生成物 1

HCID 124036918-Bromo-4-chloroquinoline

実験手順

A suspension of 2-bromoaniline (20.9 g) and 5-(methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (22.6 g) in 2-propanol (240 ml) was heated to reflux for 1 hour. The reaction solution was cooled to 0° C., and the deposit was then filtrated to obtain a pale yellow solid (35.0 g). A suspension of the obtained pale yellow solid (10.0 g) in Dowtherm (100 ml) was heated at 210° C. for 1 hour. After cooling, hexane (100 ml) was added to the reaction solution, and the deposit was filtrated to obtain 8-bromoquinolin-4(1H)-one (6.3 g). Phosphorus oxychloride (5.9 ml) was added to 8-bromoquinolin-4(1H)-one (9 g), and the mixture was heated to reflux for 2 hours. The solvent was distilled off under reduced pressure, and chloroform was added to the residue. The reaction solution was neutralized with an aqueous sodium hydroxide solution with cooling in an ice bath and partitioned into organic and aqueous layers. The organic layer was washed with brine. The organic layer thus washed was dried over anhydrous sodium sulfate. Then, the solvent was distilled off, and the residue was purified by neutral silica gel column chromatography (chloroform/methanol) to obtain 8-bromo-4-chloroquinoline (8.3 g) as a white solid.

後処理

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 2 hours
  3. distillationThe solvent was distilled off under reduced pressure, and chloroform
  4. additionwas added to the residue
  5. temperaturewith cooling in an ice bath
  6. custompartitioned into organic and aqueous layers
  7. washThe organic layer was washed with brine
  8. washThe organic layer thus washed
  9. dry with materialwas dried over anhydrous sodium sulfate
  10. distillationThen, the solvent was distilled off
  11. customthe residue was purified by neutral silica gel column chromatography (chloroform/methanol)

出典と根拠

ORDレコード
ord-f4030206459a410ba87987cf37bb27da
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912181B2

反応ノート

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