Ammonia → 1-[5-Chloro-2-(methylsulfonyl)phenyl]methanamine hydrochloride

HRID 1013955Notes

Reaction equation

HRID 1013955 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:10]([CH3:13])(=[O:12])=[O:11])=[C:6]([CH:9]=1)[C:7]#[N:8].N>C(O)C.CO.[Co]>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:10]([CH3:13])(=[O:12])=[O:11])=[C:6]([CH2:7][NH2:8])[CH:9]=1

Participants

6

Procedure

(Step 3) To a solution of 5-chloro-2-(methylsulfonyl)benzonitrile obtained in Step 2 (3.8 g) in ethanol (25 ml) was added an 8N solution of ammonia in methanol (5 ml) and Raney cobalt (19 g, wet). The resulting mixture was stirred overnight at room temperature under a hydrogen atmosphere. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. To the residue were added ethanol (10 ml) and a 2 M hydrogen chloride-methanol solution (10 ml). The resulting mixture was concentrated under reduced pressure, and the residual solid was collected by filtration and washed with ethyl acetate to give 1-[5-chloro-2-(methylsulfonyl)phenyl]methanamine hydrochloride (3.6 g) as a white solid.

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. additionTo the residue were added ethanol (10 ml)
  4. concentrationThe resulting mixture was concentrated under reduced pressure
  5. filtrationthe residual solid was collected by filtration
  6. washwashed with ethyl acetate

Sources & evidence

ORD record
ord-43f5eda27a9a4db4ae668337eac452da
Source dataset
uspto-grants-2011_07
Patent number
US07982044B2

Reaction notes

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