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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548550Generated: October 28, 2026

HCID 15524951, compound → HCID 67157886, compound

https://huagongshe.com/reaction/548550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15524951HCID 15524951—
ReactantHCID 86627833HCID 86627833—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 67157886HCID 67157886—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1,3-dibromo-5-phenylethynyl-benzene (0.1 g, 0.3 mmol, intermediate 3), (4-prop-2-ynyloxy-phenoxy)-acetic acid methyl ester (66 mg, 0.3 mmol), Pd(PPh3)2Cl2 (10 mg, 0.015 mmol), CuI (16 mg, 0.008 mmol) in dry DMF (1.5 ml) and triethylamine (1.5 ml) was heated in a microwave own for 10 min at 70° C. in a sealed tube. The reaction mixture was filtered through Decalite and the filtrate was evaporated. The residue was purified on column chromatography to give {4-[3-(3-bromo-5-phenylethynyl-phenyl)-prop-2-ynyloxy]-phenoxy}-acetic acid methyl ester in 27 mg (20%) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943612B2
Source datasetuspto-grants-2011_05
ORD IDord-0e67cbd1d51c47a7b91fdfc0df8e04d4
Source noteuspto-grants-2011_05