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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412906Generated: November 1, 2026

Hydrazine hydrate (1:1) → tert-Butyl 4-(4-aminobenzyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/412906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 18538556HCID 18538556—
SolventMeOH tetrahydrofuranHCID 21899815—
Producttert-Butyl 4-(4-aminobenzyl)piperidine-1-carboxylateHCID 2187687297%

Reaction Steps

To the solution of 1-tert-butoxycarbonyl-4-(4-nitrobenzyl)piperidine (4.53 g, 14.2 mmol) in methanol-tetrahydrofuran (1:1, 100 mL) were added activated carbon (2 g) and anhydrous ferric chloride (250 mg). To the mixture was added hydrazine monohydrate (5.64 mL), and the mixture was heated for 26 hours under ref lux. The reaction mixture was cooled to room temperature, the activated carbon was filtered off. The activated carbon was washed with metahnol. The filtrate and washings were combined, and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (hexane/ethyl acetate=2/3) to give the titled compound (4 g) as colorless powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562978B1
Source datasetuspto-grants-2003_05
ORD IDord-c9ddf5b5650a42d0896f2c02b4e31953
Source noteuspto-grants-2003_05