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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(9H-Fluoren-9-yl)methyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylateHCID 15606373—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
Product(9H-Fluoren-9-yl)methyl 4-hydrazinylpiperidine-1-carboxylate hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498325B2
Source datasetuspto-grants-2009_03
ORD IDord-c53bb0e510fb4a73be010faee4a6d4a9
Source noteuspto-grants-2009_03