Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548562Generated: October 25, 2026

1-Ethynyl-4-(trifluoromethyl)benzene → HCID 67157324, compound

https://huagongshe.com/reaction/548562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-4-(trifluoromethyl)benzeneHCID 4348295—
Reactant(4-{3-[3-Bromo-5-(3-morpholin-4-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid methyl esterHCID 67157848—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 67157324HCID 67157324—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-ethynyl-4-trifluoromethyl-benzene (159 mg, 0.94 mmol), (4-{3-[3-bromo-5-(3-morpholin-4-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester (160 mg, 0.31 mmol, example 6), Pd(PPh3)2Cl2 (36 mg, 0.031 mmol), CuI (16 mg, 0.087 mmol) in dry DMF (2 ml) and triethylamine (2 ml) was heated in a microwave own for 1 hour at 60° C. in a sealed tube. The reaction mixture was filtered through Decalite and the filtrate was evaporated. The residue was purified on column chromatography using ethyl acetate/methanol mixtures to give (2-methyl-4-{3-[3-(3-morpholin-4-yl-prop-1-ynyl)-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acid methyl ester in 18 mg (10%) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943612B2
Source datasetuspto-grants-2011_05
ORD IDord-d5029b50219440909fd79c181fb5b659
Source noteuspto-grants-2011_05