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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522802Generated: November 3, 2026

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

https://huagongshe.com/reaction/1522802

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 numberUS09078887B2
Source datasetuspto-grants-2015_07
ORD IDord-3a5dee72203f421d92af339398cb74cb
Source noteuspto-grants-2015_07