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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044105Generated: November 3, 2026

Hydrochloric Acid → Ethyl 4-(4-aminophenyl)-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/2044105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantEthyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylateHCID 57489651—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductEthyl 4-(4-aminophenyl)-4-methylpiperidine-1-carboxylateHCID 5748965257%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of ethyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylate (2.0 g, 6.13 mmol), biphenyl-2-yldicyclohexylphosphine (0.054 g, 0.153 mmol), 1M LiHMDS in THF (12.26 ml, 12.26 mmol), and Pd2(dba)3 (0.056 g, 0.061 mmol) was heated in a sealed vial at 65° C. overnight. The mixture was cooled to room temperature and treated with 1N aq. HCl (30.7 mL, 30.7 mmol) and stirred for 5 min. The mixture made basic with 1N NaOH and extracted twice with methylene chloride. The combined organic extracts were concentrated and the residue was purified by MPLC (ISCO, hexane/ethyl acetate, 24+40 g stacked silica gel columns) to give 924 mg (57%) of product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586751B2
Source datasetuspto-grants-2013_11
ORD IDord-9b753626c19247bdb8e581ebbc813e03
Source noteuspto-grants-2013_11