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Hydrochloric Acid → 3-Chloro-4-isobutylbenzaldehyde

HRID 1777334
ノート
印刷プレビュー

反応式

HRID 1777334 の反応式
[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[O:10])=[CH:7][C:6]=1[N+]([O-])=O)[CH:2]([CH3:4])[CH3:3].N([O-])=O.[Na+].[ClH:20]>O>[Cl:20][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][C:5]=1[CH2:1][CH:2]([CH3:4])[CH3:3])[CH:9]=[O:10]
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

5

反応物 3

HCID 313Hydrochloric AcidHCID 23668193Sodium NitriteHCID 867151394-Isobutyl-3-nitrobenzaldehyde

生成物 1

HCID 867151403-Chloro-4-isobutylbenzaldehyde

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
2.5 °C

実験手順

4-Isobutyl-3-nitrobenzaldehyde (3.3 g, 0.0159 mol) is added to a solution of stannous chloride (8.37 g, 0.0441 mol) in concentrated hydrochloric acid (23 mL) at 0-5° C. The reaction mixture is slowly brought to 60-65° C. and is stirred at this temperature for 30 minutes. The reaction mixture is again cooled to 0-5° C. During cooling formation of solid is observed which is broken before proceeding further. Solution of sodium nitrite (1.36 g, 0.0188 mol) in demineralized water (3 mL) is added to the above reaction mixture at 0-5° C., allowed to stir for 10 minutes at this temperature. It is then poured into a slurry of cuprous chloride (3.6 g, 0.0346 mol) in demineralized water (5 mL) at 60-65° C. & stirred for 20 minutes. The reaction mixture is extracted in ethyl acetate (2×30 mL). Combined organic layer is dried over sodium sulfate and concentrated to get the crude, which is purified using column chromatography (230-400 mesh; toluene:n-hexane, 3:7) to yield 3-chloro-4-isobutylbenzaldehyde.

後処理

  1. customis slowly brought to 60-65° C.
  2. temperatureDuring cooling formation of solid
  3. stirringto stir for 10 minutes at this temperature
  4. stirringstirred for 20 minutes
  5. extractionThe reaction mixture is extracted in ethyl acetate (2×30 mL)
  6. dry with materialCombined organic layer is dried over sodium sulfate
  7. concentrationconcentrated
  8. customto get the crude, which
  9. customis purified

出典と根拠

ORDレコード
ord-d651629d4d4f40c2bb57479dc97b7df5
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09266867B2

反応ノート

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