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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880933Generated: October 30, 2026

Benzyl Bromide → Ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-hydroxybutanoate

https://huagongshe.com/reaction/1880933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-((cyclopentylamino)methyl)-2-hydroxybutanoateHCID 57955553—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-((benzyl(cyclopentyl)amino)methyl)-2-hydroxybutanoateHCID 5795565177%

Reaction Conditions

Temperature80 °C

Reaction Steps

To ethyl 2-((cyclopentylamino)methyl)-2-hydroxybutanoate (2.7 g, 12 mmol) in 50 ml of acetonitrile at room temperature, was added benzyl bromide (2.1 ml, 18 mmol) dropwise, followed by K2CO3 (5 g, 35 mmol). The reaction mixture was heated at 80° C. for 18 h. It was then diluted to EtOAc, washed by brine and water. Organic extract dried and concentrated to a residue, which was purified on silica gel column chromatographically (Hex/EtOAc=100:1 to 4:1) to give 2.9 g product (77%). [M+H] calc'd for C19H29NO3, 320; found 320.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-8bda5367c9aa4349ad4fe0ed1fca0d97
Source noteuspto-grants-2012_11