HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173851Generated: October 27, 2026
Hydrazine hydrate (1:1) → 4-Dipropylaminomethyl-aniline
https://huagongshe.com/reaction/1173851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | (4-Nitrobenzyl)dipropylamine | HCID 15871689 | — |
| Catalyst | Trichloroiron;hexahydrate | HCID 16211236 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Dipropylaminomethyl-aniline | HCID 16777011 | 101.7% |
Reaction Steps
The compound (492 mg) obtained in Example 19-1 was dissolved in methanol (5.0 ml) and THF (2.5 ml). Then, the solution was added with activated carbon (49.0 mg) and iron trichloride hexahydrate (manufactured by Kanto Kagaku) (4.90 mg), followed by refluxing under heating for 30 minutes. After the solution was cooled to room temperature, hydrazine monohydrate (0.35 ml) was added to the solution and then the whole was refluxed for 3 hours under heat. After completion of the reaction, the reaction product was filtrated through Celite and the solvent was then distilled off. After the addition of water, chloroform extraction was performed. The extract was dried with anhydrous magnesium sulfate. The solvent was distilled off, thereby obtaining the subject compound (437 mg) as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833991B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b9f756745af74daf8053464ce7283527 |
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| Source note | uspto-grants-2010_11 |
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