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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602158Generated: October 26, 2026

Potassium Carbonate → Methyl 2-[3-(tert-butoxycarbonylamino)piperidin-1-yl]benzoate

https://huagongshe.com/reaction/602158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 2-fluoro-, methyl esterHCID 67854—
Reactant3-(Boc-amino)piperidineHCID 4233041—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-[3-(tert-butoxycarbonylamino)piperidin-1-yl]benzoateHCID 5899263520%

Reaction Conditions

Temperature130 °C

Reaction Steps

3-(tert-Butoxycarbonylamino)piperidine (7.07 g, 35.3 mmol) was dissolved in N,N-dimethylformamide (120 mL). To this solution, potassium carbonate (9.80 g, 70.9 mmol) and methyl 2-fluorobenzoate (5.0 mL, 39.2 mmol) were added and the mixture was stirred at 130° C. for 8 hours. Subsequently, the mixture was allowed to cool, diluted with ethyl acetate, and washed sequentially with water and brine. The washed product was dried over sodium sulfate and the solvent was evaporated. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=10:1->5:1) gave 2.34 g (20%) of the desired compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-9dc8db3ce1484354a405ca619454793f
Source noteuspto-grants-2011_03