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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987278Generated: October 25, 2026

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

https://huagongshe.com/reaction/1987278

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 numberUS07550489B2
Source datasetuspto-grants-2009_06
ORD IDord-eeb26fa5ef304b9f98e4fc980df6e572
Source noteuspto-grants-2009_06