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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Ethyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylate | HCID 57489651 | — |
| Catalyst | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | Ethyl 4-(4-aminophenyl)-4-methylpiperidine-1-carboxylate | HCID 57489652 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586751B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-9b753626c19247bdb8e581ebbc813e03 |
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| Source note | uspto-grants-2013_11 |
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