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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802336Generated: October 25, 2026

Potassium Phosphate, Tribasic → 3-Cyclopropyl-4-methoxybenzonitrile

https://huagongshe.com/reaction/1802336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant3-Bromo-4-methoxybenzonitrileHCID 736049—
ReactantCyclopropylboronic acidHCID 2760897—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product3-Cyclopropyl-4-methoxybenzonitrileHCID 57484707—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-bromo-4-methoxybenzonitrile (2-1, 5.0 g, 23.6 mmol, 1.0 eq), aqueous potassium phosphate tribasic (65.0 ml, 1.27 M, 3.5 eq), cyclopropylboronic acid (10.1 g, 118 mmol, 5.0 eq), Pd(OAc)2 (0.539 g, 2.36 mmol, 0.1 eq) and tricyclohexylphosphine (0.661 g, 2.36 mmol, 0.1 eq) was stirred in degassed toluene (103 ml) and heated to 80° C. for three hours. An additional amount of cyclopropylboronic acid (1.0 g, 1.16 mmol, 0.5 eq) was added and the solution was further heated for 16 hours at 80° C. to complete the reaction. The reaction mixture was cooled and partitioned between brine and EtOAc. The organic phase was dried over sodium sulfate, filtered and concentrated to give an orange oil. The oil was purified by normal phase column chromatography (0 to 10% EtOAc in hexanes) to afford the product (2-2) as a yellow oil. 1H NMR (CDCl3) δ 7.44 (dd, 1H, J=8.4, 2.0 Hz), 7.09 (d, 1H, J=2.0 Hz), 6.86 (d, 1H, J=8.4 Hz), 3.92 (s, 3H), 2.13 (m, 1H), 0.97 (m, 2H), 0.65 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349872B2
Source datasetuspto-grants-2013_01
ORD IDord-689d1f1932e3475180e0b19bdc0b1afd
Source noteuspto-grants-2013_01