HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816334Generated: October 31, 2026
Sodium Carbonate → Tert-butyl 4-(4-cyanophenyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1816334
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,1-Dimethylethyl 4-[4-(aminocarbonyl)phenyl]-1-piperidinecarboxylate | HCID 22492904 | — |
| Reactant | Phosphoryloxychloride | HCID 86587839 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-(4-cyanophenyl)piperidine-1-carboxylate | HCID 22492960 | 99.6% |
Reaction Steps
To a solution of tert-butyl 4-[4-(aminocarbonyl)phenyl]-1-piperidinecarboxylate (3.34 g) in DMF (18 ml) was dropwise added phosphoryloxychloride (3.07 ml) keeping under 10° C. with stirring and the mixture was stirred at ambient temperature for 10 minutes. The reaction mixture was poured into a mixture of saturated aqueous sodium carbonate (60 ml) and ice-water (250 ml) with stirring and extracted twice with a mixture of ethyl acetate (200 ml) and hexane (80 ml). The extract was washed twice with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The resulting residue was chromatographed on silica gel (300 ml) eluting with a mixture of n-hexane and ethyl acetate (4:1 v/v). The fractions containing the desired compound were collected and evaporated under reduced pressure to give tert-butyl 4-(4-cyanophenyl)-1-piperidine carboxylate (3.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884774B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-50dcbdd26431424fb9703970ffb4b897 |
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| Source note | uspto-grants-2005_04 |
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