HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680821Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 23454750, compound
https://huagongshe.com/reaction/1680821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 23454748 | HCID 23454748 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23454750 | HCID 23454750 | — |
Reaction Steps
The mixture of 6.0 g of 1-(4-methoxy-7 -chloro-2-phenyl-3-benzofuryl)-4-methylpiperazine hydrochloride, 45 ml of hydrazine hydrate, 250 ml of ethanol and 1.5 g of 10% palladium on charcoal is stirred at reflux for 2 hours. It is filtered, the filtrate evaporated, the residue taken up in methylene chloride and successively washed with 2 N aqueous sodium hydroxide and saturated aqueous sodium chloride, dried and evaporated. The residue is taken up in isopropanol, the solution acidified with ethereal hydrogen chloride and the precipitate collected to yield the 1-(4-methoxy-2-phenyl-3-benzofuryl)-4-methylpiperazine hydrochloride melting at 279°-282° with decomposition. This elimination of chlorine from said 7-position ensures that the process according to Example 1 provided said 4-methoxy-starting material (identified in Example 9, No. 33) unambiguously.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04276294 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-111b3ba39aa545c1b39c05b955b99c58 |
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| Source note | uspto-grants-1981_06 |
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