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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632578Generated: October 29, 2026

Ethyl Acetate → 1-Cyclopentyl 1-{[3-(bromomethyl)benzyl]amino}cyclopentanecarboxylate

https://huagongshe.com/reaction/632578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(Bromomethyl)benzaldehydeHCID 7127825—
Reactant1-Cyclopentyl 1-aminocyclopentanecarboxylateHCID 58139022—
Solvent1,1-DichloroethaneHCID 6365—
Product1-Cyclopentyl 1-{[3-(bromomethyl)benzyl]amino}cyclopentanecarboxylateHCID 8668642861.2%

Reaction Steps

To a solution of 3-(bromomethyl)-benzaldehyde (0.467 g, 2.44 mmol) in dichloroethane (20 mL) was added cycloleucine cyclopentyl ester (0.802 g, 4.06 mmol) and sodium triacetoxyborohydride (1.18 g, 5.56 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (200 mL) and washed with saturated ammonium chloride solution (3 times 50 mL). The organic fraction was dried (MgSO4), concentrated and purified by flash column chromatography (SiO2, 7:3 heptane:ethyl acetate) to yield the desired product (0.568 g, 61% yield). LC/MS: m/z 380/382 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321718B2
Source datasetuspto-grants-2016_04
ORD IDord-a5cf8c47bc324d9b8255c00db019dcb4
Source noteuspto-grants-2016_04