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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880913Generated: October 30, 2026

Benzyl Bromide → Ethyl 3-(benzyl(cyclopentyl)amino)-2-hydroxy-2-methylpropanoate

https://huagongshe.com/reaction/1880913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-(cyclopentylamino)-2-hydroxy-2-methylpropanoateHCID 57955584—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-(benzyl(cyclopentyl)amino)-2-hydroxy-2-methylpropanoateHCID 5795562677%

Reaction Conditions

Temperature80 °C

Reaction Steps

To ethyl 3-(cyclopentylamino)-2-hydroxy-2-methylpropanoate (3.9 g, 18 mmol) in 50 ml of acetonitrile at room temperature, was added benzyl bromide (3.2 ml, 27.2 mmol) dropwise, followed by K2CO3 (7.5 g, 54.3 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 10:1) to give 4.2 g product (77%). [M+H] calc'd for C18H27NO3, 306; found 306.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-6df4d33aff5a4f7993c377868b0cbf96
Source noteuspto-grants-2012_11