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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133450Erstellt: 24. Oktober 2026

Cyclobutylcarbinol → Methyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoate

https://huagongshe.com/de/reaction/133450

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclobutylcarbinolHCID 78130—
EduktMethyl 2-diazo-3-(4-chlorophenyl)propanoateHCID 73879458—
LösungsmittelBenzeneHCID 241—
ProduktMethyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoateHCID 22270441—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 500 mg (2.23 mmol) of methyl-2-diazo-3-(4-chlorophenyl)propanoate (obtained from Step A) and 1.05 mL (5 eq; 11.1 mmol) of cyclobutanemethanol in 5 mL benzene in a pressure tube was added 10 mg (1 mole %) of Rh2(OAc)4 catalyst. The tube was sealed and heated to 90° C. for 1.5 h. The solvents were evaporated under reduced pressure and the crude material was taken up in CH2Cl2 and purified by flash chromatography via gradient elution using mixtures of hexane and EtOAc (100:1 to 50:1). This provided the title compound as a clear oil. TLC Rf=0.53 (4:1 hexanes:EtOAc). 500 MHz 1H NMR (CDCl3): δ 1.68 (m, 2H); 1.85 (m, 1H); 1.88 (m, 1H); 2.01 (m, 2H); 2.53 (sep, 1H); 2.98 (m, 2H); 3.24 (dd, 1H); 3.58 (dd, 1H); 3.76 (s, 3H); 3.98 (dd, 1H); 7.20 (d, 2H); 7.28 (d, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390835B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-3e7bf8543f6a4dd487f5a453cadb89a9
Quellennotizuspto-grants-2008_06