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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749002Generated: October 30, 2026

1,3,5-Tribromobenzene → HCID 59323507, compound

https://huagongshe.com/reaction/1749002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-TribromobenzeneHCID 12279—
Reactant4-Pentyn-1-olHCID 79346—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 59323507HCID 5932350774%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,3,5-Tribromobenzene (10 g, 31.76 mmol), 4-pentyn-1-ol (10.69 g, 127.06 mmol) and bis(triphenylphosphine)palladium(II) dichloride were stirred in triethylamine under nitrogen for 5 minutes. Copper(I) iodide (92 mg, 0.48 mmol) was added and the mixture was stirred for 6 hours at 80° C. The mixture was cooled to room temperature, filtered through a celite pad and rinsed with ethyl acetate. The combined filtrate was evaporated to dryness under reduced pressure. The resulting residue was purified by column chromatography (CHCl3:MeOH 10:1) to afford 7.61 g of 1,3,5-tris-(5-hydroxy-1-pentynyl)benzene. Yield: 74%. 1H NMR (300 MHz, CDCl3) δ 7.31 (3, 3 h), 3.81 (t, J=6.0 Hz, 6H), 2.52 (t, J=6.9 Hz, 6H), 1.85 (m, 6H); 13C NMR (75 MHz, CDCl3) δ 133.8, 124.2, 90.5, 80.0, 61.9, 31.5, 16.2 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09155733B2
Source datasetuspto-grants-2015_10
ORD IDord-7c3ac73f50e04f40953c4d66ca2237c5
Source noteuspto-grants-2015_10