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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205001Generated: October 26, 2026

Dimethylformamide → Benzyl 6-(tert-butoxycarbonylamino)hexanoate

https://huagongshe.com/reaction/2205001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 6-(tert-butoxycarbonylamino)hexanoateHCID 12160267—

Reaction Steps

To a solution of 6-(tert-butoxycarbonylamino)hexanoic acid (1 eq) in acetone (0.2 M) was added potassium carbonate (2 eq) and (bromomethyl)benzene (2 eq) in acetone (2 M). The reaction mixture was stirred at room temperature for 1 hour. Additional amount of DMF was then added to the reaction mixture to facilitate the dissolution of potassium carbonate. The reaction mixture was stirred at room temperature for another 30 minutes. The mixture was then diluted with ethyl acetate, and washed with 5% citric acid, water and brine. The organic layer was dried over anhydrous Na2SO4, and concentrated en vaccuo. The crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 10-40% EtOAc/Hex to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365506B2
Source datasetuspto-grants-2016_06
ORD IDord-35a4fcc3c65944a18cada0ca48c8014d
Source noteuspto-grants-2016_06