HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633412Generated: October 26, 2026
Hydrochloric Acid → 4-(4-Nitro-2-(trifluoromethyl)phenoxy)piperidine
https://huagongshe.com/reaction/633412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate | HCID 22181018 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4-Nitro-2-(trifluoromethyl)phenoxy)piperidine | HCID 20735381 | 90% |
Reaction Steps
A solution of tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate (1.4 g, 1.0 eq, 3.6 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. while stifling. 4N HCl in dioxane (15 mL) was added to the above solution and stirred at 0° C. for 30 minutes and brought to room temperature for 2 hours. The volatiles were removed under vacuum to leave a crude solid. The crude mixture was dissolved in EtOAc (100 mL) and partitioned with 1N aqueous NaOH solution (50 mL). Organic layers were separated and the aqueous layer was washed with EtOAc (50 mL). The combined organic layers were dried over Na2SO4 and concentrated under vacuum to give the desired product in 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321763B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-36f697c62a644954a1072d4dac02887d |
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| Source note | uspto-grants-2016_04 |
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