HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832220Generated: October 27, 2026
Water → Tert-butyl 4-[3-(propionylamino)phenyl]-1-piperidinecarboxylate
https://huagongshe.com/reaction/1832220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | tert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylate | HCID 22049268 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-[3-(propionylamino)phenyl]-1-piperidinecarboxylate | HCID 22049473 | 104.1% |
Reaction Steps
Propionyl chloride (5.53 g, 0.0597 mol) was added dropwise to a solution of tert-butyl 4-(3-aminophenyl)-1-piperidinecarboxylate (15.0 g, 0.0543 mol) and TEA (16.5 g, 0.163 mol) in THF (200 mL) and the mixture was stirred at room temperature for 3 h. Water (50 mL) was added to the reaction mixture, the aqueous layer was extracted with CH2Cl2 (3×100 mL), and the combined organic extracts were washed with brine (50 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by chromatography on silica using hexane/EtOAc (10:1) to afford the product (18.8 g, 99%). 1H NMR (400 MHz, CDCl3) δ 7.48 (s, 1H) 7.34–7.21 (m, 3H), 6.93 (d, 1H, J=7.4 Hz), 2.77 (t, 2H, J=11.5 Hz), 2.68–2.58 (m, 1H), 2.38 (q, 2H, J=7.6 Hz), 1.87–1.67 (m, 4H), 1.67–1.54 (m, 2H), 1.48 (s, 9H), 1.25 (t, 3H, J=7.5 Hz); ESMS m/e: 333.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067534B1 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-421dc3d39e8b40e69b90906c1289b02c |
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| Source note | uspto-grants-2006_06 |
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