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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381055Generated: November 2, 2026

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

https://huagongshe.com/reaction/2381055

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 rt, 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 numberUS08258154B2
Source datasetuspto-grants-2012_09
ORD IDord-879d427706014e30ab405d745ee1c5e3
Source noteuspto-grants-2012_09