Hydrochloric Acid → N-[(4-hydrazinylphenyl)methyl]methanesulfonamide hydrochloride
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:4][CH:3]=1.[N:14]([O-])=O.[Na+].[ClH:18]>O>[ClH:18].[NH:1]([C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:4][CH:3]=1)[NH2:14]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -55 °C
Procedure
To a suspension of 18.0 g (89.9 mmol, 1.0 equiv.) of N-[(4-aminophenyl)methyl]methanesulfonamide in 85 ml of water and 175 mL of concentrated aqueous hydrochloric acid at 0° C. was added a solution of 6.21 g (89.9 mmol, 1.0 equiv.) of sodium nitrite in 85 mL of water. The reaction mixture was stirred for fifteen minutes. Meanwhile a solution of 101.6 g of stannous chloride dihydrate in 175 mL of concentrated aqueous hydrochloric acid was prepared and cooled to -55° C. The solution of the diazonium salt was filtered into the stannous chloride solution. The reaction was maintained between -55° C. and -35° C. for one hour. The crystalline material was collected by filtration and dried under high vacuum at 65° C. for 16 hours to yield 23.9 g (>100%) of crude N-[(4-hydrazinylphenyl)methyl]methanesulfonamide hydrochloride.
Workup
- filtrationThe solution of the diazonium salt was filtered into the stannous chloride solution
- temperatureThe reaction was maintained between -55° C. and -35° C. for one hour
- filtrationThe crystalline material was collected by filtration
- customdried under high vacuum at 65° C. for 16 hours
Sources & evidence
- ORD record
- ord-c413995b1f7f4a038b002cf96e6db12f
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05434154
Reaction notes
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