Hydrochloric Acid → 7-Methyl-1,3-benzothiazol-6-amine

HRID 1275096Notes

Reaction equation

HRID 1275096 reaction equation
Cl[Sn]Cl.Cl.[CH3:5][C:6]1[C:14]2[S:13][CH:12]=[N:11][C:10]=2[CH:9]=[CH:8][C:7]=1[N+:15]([O-])=O.[OH-].[Na+]>>[CH3:5][C:6]1[C:14]2[S:13][CH:12]=[N:11][C:10]=2[CH:9]=[CH:8][C:7]=1[NH2:15]

Participants

5

Conditions

Temperature
25 °C

Procedure

To a solution of SnCl2 (3.0 g, 3.8 mmol) and 10 mL of con.HCl was added 7-methyl-6-nitrobenzothiazole (0.68 g, 3.5 mmol) in a portion and the resulting reaction mixture was stirred for 1 h at 25° C. The reaction mixture was basified with aqueous NaOH and extracted with EtOAc and CHCl3. Combined organic layers were dried over Na2SO4 and concentrated in vacuo, yielding an oil (0.65 g, >95%) which was identified as the desired amine and subjected to a following reaction without further purification.

Workup

  1. customthe resulting reaction mixture
  2. extractionextracted with EtOAc and CHCl3
  3. dry with materialCombined organic layers were dried over Na2SO4
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ae164dd892e34b0cb20e3555f2cd3fff
Source dataset
uspto-grants-2000_12
Patent number
US06159998

Reaction notes

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