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Hydrochloric Acid → 1-Chlorononan-4-one

HRID 46960
ノート
印刷プレビュー

反応式

HRID 46960 の反応式
[CH2:1](Br)[CH2:2][CH2:3][CH2:4][CH3:5].[Mg].[Cl:8][CH2:9][CH2:10][CH2:11][C:12]#N.Cl.CC[O:17]CC>>[Cl:8][CH2:9][CH2:10][CH2:11][C:12](=[O:17])[CH2:1][CH2:2][CH2:3][CH2:4][CH3:5]
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 5

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 80571-BromopentaneHCID 123364-ChlorobutyronitrileHCID 5462224Magnesium

生成物 1

HCID 203861031-Chlorononan-4-one

実験手順

To the Grignard reagent prepared from a mixture of amyl bromide (226.59 g.; 1.5 moles) and magnesium (36.48 g.; 1.5 moles) in ether (1000 ml.) is added, dropwise, during one hour, 4-chlorobutyronitrile (155.34 g.; 1.5 moles). Stirring is continued for an additional one hour. The reaction mixture is poured into a mixture of finely crushed ice (1000 g.) and concentrated hydrochloric acid (750 ml.). The ether layer is separated quickly and discarded. The aqueous layer is heated on a steam bath for one hour to hydrolyze the intermediate imine and cause the separation of the ketone as an oil. After cooling, the oil is extracted with ether and the combined extracts are washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is removed under vacuum and the residual oil is distilled to give 69.0 g. (26%) of colorless oil, b.p. 115°-117° C./14 mm.; pmr (CDCl3) δ 0.090 (3H,t), 3.56 (2H,t,CH2Cl).

後処理

  1. additionis added
  2. waitis continued for an additional one hour
  3. customThe ether layer is separated quickly
  4. temperatureThe aqueous layer is heated on a steam bath for one hour
  5. customthe separation of the ketone as an oil
  6. temperatureAfter cooling
  7. extractionthe oil is extracted with ether
  8. washthe combined extracts are washed with saturated sodium chloride solution
  9. dry with materialdried over anhydrous sodium sulfate
  10. customThe solvent is removed under vacuum
  11. distillationthe residual oil is distilled
  12. customto give 69.0 g

出典と根拠

ORDレコード
ord-a0aa2a6d84ee47cc9acefa3def131aec
出典データセット
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04175203

反応ノート

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