HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782685Generated: October 30, 2026
Hydrochloric Acid → (9H-Fluoren-9-yl)methyl 4-hydrazinylpiperidine-1-carboxylate hydrochloride
https://huagongshe.com/reaction/1782685
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (9H-Fluoren-9-yl)methyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylate | HCID 15606373 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (9H-Fluoren-9-yl)methyl 4-hydrazinylpiperidine-1-carboxylate hydrochloride | HCID 18321221 | — |
Reaction Steps
21.8 g (0.0498 mol) of N-(1,1-dimethylethoxycarbonyl)-N′-[1-(9H-fluoren-9-ylmethoxycarbonyl)-4-piperidinyl]-hydrazine were dissolved in 100 ml of trifluoroacetic acid and stirred for 1 hour at room temperature. The excess trifluoroacetic acid was removed in vacuo, the residue was dissolved in 50 ml of water and made alkaline with 10% aqueous sodium carbonate solution. The solution was extracted thoroughly with dichloromethane, the combined extracts were dried over magnesium sulphate and evaporated down in vacuo. The residue thus obtained was taken up in ethyl acetate and converted into the hydrochloride by the addition of ethereal hydrogen chloride solution. After recrystallisation from anhydrous ethanol 6.2 g (33.3% of theory) of colourless crystals of melting point 160-162° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498325B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c53bb0e510fb4a73be010faee4a6d4a9 |
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| Source note | uspto-grants-2009_03 |
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