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Nitric Acid → 1-Nitro-3-(pentafluoroethyl)benzene

HRID 1414508
ノート
印刷プレビュー

反応式

HRID 1414508 の反応式
[F:1][C:2]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([F:7])[C:3]([F:6])([F:5])[F:4].[N+:14]([O-])([OH:16])=[O:15].S(=O)(=O)(O)O>>[N+:14]([C:10]1[CH:9]=[C:8]([C:2]([F:7])([F:1])[C:3]([F:5])([F:4])[F:6])[CH:13]=[CH:12][CH:11]=1)([O-:16])=[O:15]
参加物反応条件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 944Nitric AcidHCID 1118Sulfuric AcidHCID 11298517(Pentafluoroethyl)benzene

生成物 1

HCID 232334121-Nitro-3-(pentafluoroethyl)benzene

反応条件

温度
45 °C

実験手順

74 G. (0.4 moles) of pentafluoroethylbenzene is cooled to 5° C. and treated dropwise with a mixture of 22 g. (0.33 moles) of concentrated nitric acid and 33 g. (0.32 moles) of concentrated sulfuric acid. The temperature is maintained at 5°-15° C. during the 1 hour addition period and then raised to 45° C. for 1 hour. The reaction mixture is cooled and poured onto ice. The aqueous mixture is extracted with ether, the ether extracts washed with water, dried over sodium sulfate, and the residue is distilled at 0.35 mm. of Hg at 74°-75° C. The yield is 84 g. (87%) of m-nitro-pentafluoroethylbenzene.

後処理

  1. additiontreated dropwise with a mixture of 22 g
  2. temperatureThe temperature is maintained at 5°-15° C. during the 1 hour addition period
  3. temperatureThe reaction mixture is cooled
  4. additionpoured onto ice
  5. extractionThe aqueous mixture is extracted with ether
  6. washthe ether extracts washed with water
  7. dry with materialdried over sodium sulfate
  8. distillationthe residue is distilled at 0.35 mm. of Hg at 74°-75° C

出典と根拠

ORDレコード
ord-90381090dab340e99c6bd3cef3c8bccc
出典データセット
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04001406

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート