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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383349Generated: October 26, 2026

Sodium Carbonate → 2-(Cyclopent-1-en-1-yl)-4-fluoro-1-methoxybenZene

https://huagongshe.com/reaction/383349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-4-fluoroanisoleHCID 136292—
Reactant(Cyclopent-1-en-1-yl)boronic acidHCID 3861343—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product2-(Cyclopent-1-en-1-yl)-4-fluoro-1-methoxybenZeneHCID 5939493449.2%

Reaction Steps

A microwave vial was charged with 2-bromo-4-fluoro-1-methoxybenzene (500 mg, 2.44 mmol), 1-cyclopentenylboronic acid (273 mg, 2.44 mmol), and Pd(dppf)Cl2 (199 mg, 0.24 mmol). The solids were dissolved in acetonitrile (7 mL) and 2 M Na2CO3 (5 mL) and the mixture heated under microwave irradiation for 20 min at 110° C. The reaction was diluted with dichloromethane (50 mL) and the layers separated. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. Purification by silica gel chromatography (10-30% ethyl acetate/hexane) provided 2-cyclopentenyl-4-fluoro-1-methoxybenzene (231 mg, 49% yield). 1H NMR (400.0 MHz, DMSO-d6) δ 7.01 (dd, J=3.1, 10.0 Hz, 1H), 6.92-6.82 (m, 1H), 6.54 (dd, J=2.4, 6.5 Hz, 1H), 6.54 (s, 1H), 3.87 (s, 3H), 2.78-2.73 (m, 2H), 2.62-2.57 (m, 2H), 2.03-1.95 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367660B2
Source datasetuspto-grants-2013_02
ORD IDord-6f855cbf05f34ea5b1929c1c4412c1d3
Source noteuspto-grants-2013_02