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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1948568Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1948568

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktTricyclohexylphosphineHCID 75806—
Edukt3-Bromo-4-methoxybenzonitrileHCID 736049—
EduktCyclopropylboronic acidHCID 2760897—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
Produkt3-Cyclopropyl-4-methoxybenzonitrileHCID 57484707—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 3-bromo-4-methoxybenzonitrile (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 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399494B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-ae4f2c98f52b405c9a0561796238fb85
Quellennotizuspto-grants-2013_03