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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541270Generated: November 1, 2026

Methyl 4-bromo-2-methylbenzoate → Methyl 4-cyclobutyl-2-methylbenzoate

https://huagongshe.com/reaction/541270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromo-2-methylbenzoateHCID 22031226—
ReactantHCID 178419766HCID 178419766—
ProductMethyl 4-cyclobutyl-2-methylbenzoateHCID 10488418—

Reaction Conditions

Temperature65 °C

Reaction Steps

Cyclobutylzinc(II) bromide (50 ml, 0.5 M in THF, 25.0 mmol) was added to a mixture of methyl 4-bromo-2-methylbenzoate (compound 152.1, 5.2 g, 22.7 mmol) and PdCl2(dppf)CH2Cl2 (1.85 g, 2.27 mmol). The mixture was degassed and the flask was filled with argon through a balloon. The mixture was heated at 65° C. under argon for 24 hours. The mixture was cooled to 0° C. and quenched with water (10 ml). The mixture was diluted with EtOAc (200 ml), washed with water then with brine. The EtOAc layer was dried (Na2SO4), concentrated under reduced pressure, and purified using column (silica gel) chromatography (hexanes:EtOAc 30:1 to 20:1). Yield: 4.1 g, clear oil, 89.1%. 1H NMR (400 MHz, Chloroform-d) δ 7.86 (d, 1H), 7.12-7.02 (m, 2H), 3.88 (s, 3H), 3.59-3.48 (m, 1H), 2.59 (s, 3H), 2.35 (m, 2H), 2.22-1.96 (m, 3H), 1.86-1.84 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-27c91103071f4ea8a07639c0cc26aa8e
Source noteuspto-grants-2014_10