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Phosphorus oxychloride → 4-Fluoro-3-nitrobenzene-1-sulfonyl chloride

HRID 1512986
ノート
印刷プレビュー

反応式

HRID 1512986 の反応式
P(Cl)(Cl)(Cl)=O.[F:6][C:7]1[CH:12]=[CH:11][C:10]([S:13](O)(=[O:15])=[O:14])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18].P(Cl)(Cl)(Cl)(Cl)[Cl:21]>>[F:6][C:7]1[CH:12]=[CH:11][C:10]([S:13]([Cl:21])(=[O:15])=[O:14])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18]
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 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 774984-Fluoro-3-nitrobenzenesulfonic acid

生成物 1

HCID 27827994-Fluoro-3-nitrobenzene-1-sulfonyl chloride収率 81.7%

実験手順

To 2-fluoronitrobenzene (2.33 g) was added fuming sulfuric acid (20 mL), and the mixture was stirred at 60° C. for 30 minutes. The reaction mixture was cooled to room temperature. The reaction mixture was poured into ice and potassium chloride (10 g), and the resulting mixture was stirred at room temperature for 30 minutes. The precipitated crystals were collected by filtration. The collected crystals were washed with water, and dried under reduced pressure to give 4-fluoro-3-nitrobenzenesulfonic acid (3.15 g). To phosphoryl chloride (85 mL) were added 4-fluoro-3-nitrobenzenesulfonic acid (3.15 g) and phosphorus pentachloride (2.82 g) under ice-cooling, and the mixture was heated at reflux overnight. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. To the residue was added ice water, and the resulting mixture was extracted with diethyl ether. The extract was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane−n-hexane/ethyl acetate=3/1) to give the title compound (2.65 g).

後処理

  1. temperaturecooling
  2. temperaturethe mixture was heated
  3. temperatureat reflux overnight
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added ice water
  6. extractionthe resulting mixture was extracted with diethyl ether
  7. washThe extract was washed with brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customThe solvent was removed under reduced pressure
  10. customthe residue was purified by column chromatography on silica gel (eluent: n-hexane−n-hexane/ethyl acetate=3/1)

出典と根拠

ORDレコード
ord-23949fc348c44aca8b1d17a8fa83058d
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08217069B2

反応ノート

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