HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884471Generated: October 30, 2026
Hydrazine hydrate (1:1) → N1-(3-Morpholinopropyl)benzene-1,4-diamine
https://huagongshe.com/reaction/1884471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21975327 | HCID 21975327 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N1-(3-Morpholinopropyl)benzene-1,4-diamine | HCID 21974739 | — |
Reaction Steps
A suspension of 5.00 gms. of (3-morpholin-4-yl-propyl)-(4-nitro-phenyl)-amine in 110 mL of ethanol is heated to 50° C. Once dissolution is achieved 5.49 mL hydrazine monohydrate is added to the solution. A Raney nickel slurry in water is added to the 50° C. solution dropwise, waiting after each addition for the bubbling to cease. Sufficient quantities of Raney nickel have been added when continued addition of Raney nickel causes no further gas evolution. The reaction is then maintained at 50° C. for an additional hour, and subsequently is cooled to room temperature. The reaction mixture is filtered through a pad of celite (rinsing the pad with methanol). N-(3-Morpholin-4-yl-propyl)-benzene-1,4-diamine (4.39 gms.) is isolated upon evaporation of the filtrate, and is subsequently used without purification in the reaction of Example 297.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06765012B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-9381d299fdaa4effa0048ec30dd2d779 |
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| Source note | uspto-grants-2004_07 |
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