Hydrazine hydrate (1:1) → (6-Hydrazinopyridin-3-yl)methanol
Reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][CH:3]=1.O.[NH2:11][NH2:12]>>[NH:11]([C:2]1[N:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][CH:3]=1)[NH2:12]Participants
3
Procedure
20.0 g (139 mmol) (6-chloropyridin-3-yl)methanol are heated under reflux overnight in 400 ml of a 35% strength aqueous hydrazine hydrate solution. The mixture is concentrated, toluene is added, the mixture is concentrated again and the residue is stirred with a mixture of methylene chloride, methanol and diethyl ether. The crystalline residue (hydrazine hydrochloride) is filtered off, the filtrate is concentrated and the residue is dried in vacuo.
Workup
- concentrationThe mixture is concentrated
- additiontoluene is added
- concentrationthe mixture is concentrated again
- filtrationThe crystalline residue (hydrazine hydrochloride) is filtered off
- concentrationthe filtrate is concentrated
- customthe residue is dried in vacuo
Sources & evidence
- ORD record
- ord-a13aa0cd6eef4a0db6c93ce4bedad483
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252817B2
Reaction notes
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