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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488603Generated: October 25, 2026

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

https://huagongshe.com/reaction/488603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutylcarbinolHCID 78130—
ReactantMethyl 2-diazo-3-(4-chlorophenyl)propanoateHCID 73879458—
SolventBenzeneHCID 241—
ProductMethyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoateHCID 22270441—

Reaction Conditions

Temperature90 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972295B2
Source datasetuspto-grants-2005_12
ORD IDord-8567460ae4f24b699bc527160b311e79
Source noteuspto-grants-2005_12