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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914162Generated: October 31, 2026

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

https://huagongshe.com/reaction/914162

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 numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-0d15590e959a43d39dae2870566636f9
Source noteuspto-grants-2011_09