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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914142Generated: October 30, 2026

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

https://huagongshe.com/reaction/914142

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 numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-00f69cd42da5432aaad907a0cb1e5701
Source noteuspto-grants-2011_09