HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232890Generated: October 31, 2026
Hydrochloric Acid → HCID 23361185, compound
https://huagongshe.com/reaction/232890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23361122 | HCID 23361122 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23361185 | HCID 23361185 | — |
Reaction Steps
To a solution of 3.0 g of 1'-trifluoroacetyl-3,4-dihydro-7-nitrospiro[naphthalene-2(1H),2'-piperidine]-1-one in 50 ml of ethanol, 0.30 g of 10% palladium-carbon catalyst and 2 ml of concentrate hydrochloric acid were added, followed by 3 hours of catalytic reduction at normal pressure and temperature. After the catalyst was filtered off, the filtrate was distilled to remove the solvent. The residue was dissolved in methylene chloride and washed with water. The methylene chloride layer was dried over anhydrous magnesium sulfate and filtered, after which the solvent was distilled off. The residue was treated with 2.2 ml of 4 N-methanolic hydrochloric acid to yield a solid, which was then recrystallized from ethanol-ether to yield 2.37 g of 7-amino-1'-trifluoroacetyl-3,4-dihydrospiro[naphthalene-2(1H),2'-piperidine]-1-one hydrochloride as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591849 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-b8cfe76311324f1882ae50e184b46174 |
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| Source note | uspto-grants-1997_01 |
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