HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419570Generated: November 3, 2026
Trifluoroacetic acid methylene chloride → tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1419570
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Reactant | t-Butyl (1-t-Butoxycarbonylpiperidin-4-yl)phenylcarbamate | HCID 54392086 | — |
| Product | tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate | HCID 22266191 | — |
Reaction Steps
t-Butyl (1-t-butoxycarbonylpiperidin-4-yl)phenylcarbamate (290 mg) was dissolved in trifluoroacetic acid-dichloromethane (10%, 20 mL) and stirred at room temperature for 2 h. The solvent was evaporated under reduced pressure and the residue was partitioned between aqueous sodium hydroxide (2M) and ether (30 mL). The organic layer was separated, dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane (20 mL) and cooled in ice. Di-t-butyldicarbonate (161 mg) was added and the mixture was stirred at room temperature for 30 min. The solvent was evaporated under reduced pressure and the residue was purified by MPLC on silica gel, eluting with EtOAc/Hexane (5:95) to give the title compound as a clear oil (141 mg), δH (CDCl3) 1.55 (9H, s), 1.59 (2H, m), 1.82 (2H, m), 2.58 (1H, m), 2.77 (1H, m), 3.64 (2H, br s), 4.16 (2H, m), 6.68-6.79 (2H, m), 7.01-7.26 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885999 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-440995c7154948ddb8398d636b6b85b8 |
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| Source note | uspto-grants-1999_03 |
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