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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095762Generated: November 2, 2026

Bromocyclopentane → Methyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoate

https://huagongshe.com/reaction/1095762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-hydroxy-4-methoxy-2-nitrobenzoateHCID 59268115—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoateHCID 66781723—

Reaction Steps

A mixture of methyl 3-hydroxy-4-methoxy-2-nitrobenzoate (1.14 g, 5.0 mmol), bromocyclopentane (0.7 mL, 6.5 mmol), potassium carbonate (2.0 g, 14 mmol), and anhydrous acetonitrile (15 mL) was refluxed under N2. After 19 h, the reaction was allowed to cool to room temperature, concentrated, and purified by silica gel chromatography (4:1→3:2; hexanes:ethyl acetate) to give methyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoate: MS (ESI): 296.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138205B2
Source datasetuspto-grants-2012_03
ORD IDord-d65596030e66412eaecd3601da7b1681
Source noteuspto-grants-2012_03