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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611733Generated: November 2, 2026

Benzyl Bromide → 4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1611733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventDimethylformamideHCID 6228—
Product4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylateHCID 22255913104.1%

Reaction Steps

A solution of 1-tert-butoxycarbonyl-piperidine-4-carboxylic acid (20 g) in DMF (100 ml) was treated with anhydrous potassium carbonate (60 g) and then benzyl bromide (16.43 g) and the mixture was stirred at room temperature for 72 hours. It was filtered, evaporated to dryness, dissolved in ethyl acetate, washed with sodium carbonate solution and water and dried over sodium sulfate. The product was evaporated to give an oil (29 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989447B2
Source datasetuspto-grants-2006_01
ORD IDord-2160915f63a74c17a07eb2965f8c71a2
Source noteuspto-grants-2006_01