Ammonium Hydroxide → Ammonium Chloride
Reaction equation
[ClH:1].Cl.[NH2:3][CH2:4][CH2:5][S:6][CH2:7][C:8]1[C:13]([SH:14])=[CH:12][CH:11]=[CH:10][N:9]=1.[OH-].[NH4+:16]>O>[NH2:3][CH2:4][CH2:5][S:6][CH2:7][C:8]1[C:13]([S:14][S:14][C:13]2[C:8]([CH2:7][S:6][CH2:5][CH2:4][NH2:3])=[N:16][CH:10]=[CH:11][CH:12]=2)=[CH:12][CH:11]=[CH:10][N:9]=1.[Cl-:1].[NH4+:3]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(2-aminoethylthiomethyl)-3-mercaptopyridine dihydrochloride (0.40 g) in water (4 mL) basified with addition of concentrated ammonium hydroxide and a stream of air was bubbled through it for 16 hours. Reaction mixture was evaporated to dryness to produce solid residue of title product and ammonium chloride which was used for next step without further purification. 1H NMR (D2O) δ 2.75 (t, J=6H, 2H), 3.15 (t, J=6H, 2H), 4.00 (s, 2H), 7.38 (dd, J=4, J=6, 1H), 8.21 (d, J=6, 1H), 8.38 (d, J=4, 1H).
Workup
- customa stream of air was bubbled through it for 16 hours
- customReaction mixture
- customwas evaporated to dryness
Sources & evidence
- ORD record
- ord-fb2ded1d79674b74ba3c7c744bf411ab
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06723716B1
Reaction notes
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