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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189742Generated: October 25, 2026

1-Cyclohexenylboronic acid → 4-(1-Cyclohexen-1-yl)-3-ethylbenzonitrile

https://huagongshe.com/reaction/2189742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclohexenylboronic acidHCID 3862902—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Ethyl-4-iodobenzonitrileHCID 59316718—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventMethanolHCID 887—
Product4-(1-Cyclohexen-1-yl)-3-ethylbenzonitrileHCID 5931671681.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-ethyl-4-iodobenzonitrile (D10) (1.23 g, 4.80 mmol), 1-cyclohexen-1-ylboronic acid (907 mg, 7.20 mmol), sodium methoxide (778 mg, 14.4 mmol) and bis(triphenylphosphine)palladium (II) chloride (337 mg, 0.48 mmol) in anhydrous methanol (12 mL) was heated at 80° C. for 10 minutes in the microwave. The reaction mixture was partitioned between ethyl acetate (40 mL) and water (40 mL) before the organic layer was further washed with water (40 mL), dried (phase separator) and concentrated in vacuo. The crude material was purified by silica chromatography, eluting 0-5% EtOAc in hexane over 30 minutes to give the title compound as a yellow oil (824 mg, 3.91 mmol). δH (methanol-d4, 400 MHz) 7.56 (1H, d), 7.46 (1H, dd), 7.19 (1H, d), 5.61-5.56 (1H, m), 2.68 (2H, quart), 2.23-2.16 (4H, m), 1.85-1.68 (4H, m), 1.20 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324254B2
Source datasetuspto-grants-2012_12
ORD IDord-389ff46626c84203a490bbb175c04b79
Source noteuspto-grants-2012_12