HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499191Generated: October 26, 2026
N-Boc-3-[(1-Cbz-4-piperidyl)oxy]aniline → 1-Cbz-4-(3-aminophenoxy)-piperidine
https://huagongshe.com/reaction/499191
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Boc-3-[(1-Cbz-4-piperidyl)oxy]aniline | HCID 68454608 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1-Cbz-4-(3-aminophenoxy)-piperidine | HCID 68453441 | — |
Reaction Steps
4-(3-tert-Butoxycarbonylamino-phenoxy)-piperidine-1-carboxylic acid benzyl ester (11.8 g, 27.6 mmol) is dissolved in a solution of trifluoroacetic acid in dichloromethane (25% v/v, 20 mL). The reaction mixture is stirred at 22° C. for 60 min. After removal of the solvent, the oily residue is dissolved in dichloromethane (250 mL) and neutralized with 0.2 N aqueous sodium hydroxide solution (250 mL) and extracted with dichloromethane (10×100 mL) followed by ethyl acetate (5×100 mL). The combined organic phases are dried over anhydrous sodium sulfate. After removal of solvent, the crude product is purified on silica gel chromatography with dichloromethane-methanol to give a light brown oil (4.84 g, 54%, ES+(m/z) 327.3 [M+H]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767674B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-1423ec6a4ad149ad98a04e0a774cde5c |
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| Source note | uspto-grants-2010_08 |
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