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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274067Generated: October 31, 2026

Methyl 4-chloro-3-(trifluoromethyl)benzoate → Methyl 4-(cyclohexylmethyl)-3-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/2274067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chloro-3-(trifluoromethyl)benzoateHCID 14148738—
ReactantHCID 178419774HCID 178419774—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(cyclohexylmethyl)-3-(trifluoromethyl)benzoateHCID 6721159893.2%

Reaction Steps

To a stirred solution of methyl 4-chloro-3-(trifluoromethyl)benzoate (238 mg, 1.0 mmol) and bis(tri-t-butylphosphine)palladium (0) (51 mg, 0.10 mmol) in THF (2 mL) was added (cyclohexylmethyl)zinc(II) bromide (6 mL, 3.00 mmol) at room temperature. The reaction mixture was heated at reflux for 2 h, quenched with saturated NaHCO3 solution, filtered through Celite. The filtrate was extracted with ethyl acetate. The combined organics were dried and concentrated, and the residue was purified by column chromatography to give the title compound (280 mg) as colorless oil. LCMS m/z=301.4 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 0.96-1.06 (m, 2H), 1.14-1.22 (m, 3H), 1.62-1.72 (m, 6H), 2.71 (d, J=6.7 Hz, 2H), 3.94 (s, 3H), 7.39 (d, J=8.1 Hz, 1H), 8.10 (dd, J=8.0 and 1.5 Hz, 1H), 8.30 (d, J=1.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126932B2
Source datasetuspto-grants-2015_09
ORD IDord-4b57efbbf48043d4adfd93f9ac9d26c4
Source noteuspto-grants-2015_09