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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,1-Dimethylethyl 4-[4-(aminocarbonyl)phenyl]-1-piperidinecarboxylateHCID 22492904—
ReactantPhosphoryloxychlorideHCID 86587839—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(4-cyanophenyl)piperidine-1-carboxylateHCID 2249296099.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884774B2
Source datasetuspto-grants-2005_04
ORD IDord-50dcbdd26431424fb9703970ffb4b897
Source noteuspto-grants-2005_04