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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180973Generated: October 26, 2026

Benzoic Acid → tert-Butyl 3-(benzoylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1180973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Producttert-Butyl 3-(benzoylamino)piperidine-1-carboxylateHCID 2201703339.1%

Reaction Steps

A solution of benzoic acid (0.123 g) in DMF (5 ml) was treated with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.231 g), HOBT (0.163 g) and triethylamine (0.56 ml) and stirred at room temperature for 1 h. A solution of 3-amino-1-N-Boc-piperidine (0.3 g) in DMF (1 ml) was then added and stirring continued for 18 h. The solution was concentrated under reduced pressure to give an oil which was partitioned between ethyl acetate and water. The separated organic extracts were washed with water, hydrochloric acid (2N), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (0.120 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282497B2
Source datasetuspto-grants-2007_10
ORD IDord-db2281eb53c3413ab6f05803a40067d7
Source noteuspto-grants-2007_10