Ammonium Chloride → 3-Amino-4-chlorobenzaldehyde

HRID 1801570

Reaction equation

HRID 1801570 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[N+:10]([O-])=O.[Cl-].[NH4+]>CO.O.[Fe]>[NH2:10][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[Cl:1])[CH:6]=[O:7]

Participants

6

Procedure

To a solution of 4-chloro-3-nitrobenzaldehyde 1 (11.47 g, 62 mmol) in MeOH (230 mL) and water (85 mL) was added ammonium chloride (24.2 g, 452 mmol) and iron (18.4 g, 329 mmol). The reaction mixture was stirred at room temperature for 16 h, filtered, partially concentrated under reduced pressure, and diluted with EtOAc and water. The aqueous phase was extracted with EtOAc (3×) and the combined organic extracts were washed with brine (1×), dried over MgSO4, filtered, and concentrated in vacuo. The crude aniline was dissolved in CH2Cl2 (˜150 mL), diluted with hexanes (˜300 mL), and cooled to 0° C. The solid was collected by filtration and washed with hexanes to give 3-amino-4-chlorobenzaldehyde 2 (5.36 g, 56% yield) as a yellow solid. Mass spectrum: calculated for C7H5ClNO 155.0. found 156.1 (M++1).

Workup

  1. filtrationfiltered
  2. concentrationpartially concentrated under reduced pressure
  3. additiondiluted with EtOAc and water
  4. extractionThe aqueous phase was extracted with EtOAc (3×)
  5. washthe combined organic extracts were washed with brine (1×)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. dissolutionThe crude aniline was dissolved in CH2Cl2 (˜150 mL)
  10. additiondiluted with hexanes (˜300 mL)
  11. temperaturecooled to 0° C
  12. filtrationThe solid was collected by filtration
  13. washwashed with hexanes

Sources & evidence

ORD record
ord-2e82f5acdc734e9f9fcbd4efcf71bc94
Source dataset
uspto-grants-2013_01
Patent number
US08349831B2

Linked notes

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