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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367908Generated: October 30, 2026

Potassium Carbonate → 1-Ethynyl-4-(4-n-butylphenylethynyl)benzene

https://huagongshe.com/reaction/2367908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66776559HCID 66776559—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1-Ethynyl-4-(4-n-butylphenylethynyl)benzeneHCID 858121898.2%

Reaction Steps

1-(trimethylsilylethynyl)-4-(4-n-butylphenylethynyl)benzene (192 g, 11.86 mmol) was dissolved in CH2Cl2 (100 nit) diluted with MeOH (40 mL) and then treated with powdered K2CO3 (2.1 g, 15 mmol) and allowed to stir at ambient temperature for 19 h under N2. The reaction mixture was filtered to remove solids, concentrated, redissolved in CHCl3, washed with water (2×), brine, dried over MgSO4, filtered and concentrated to dryness to give a brown solid. The solid was chromatographed on silica gel, eluting with 15:1 hexanes/EtOAc to give several fractions rich in product. These fractions were combined and chromatographed again with 95:5 hexanes/EtOAc to give 0.25 g (7%) product as a waxy solid. 1H NMR (CDCl3) δ: 7.50 (s, 4H), 7.47 (d, 8.2 Hz, 2H); 7.21 (d, J=8.2 Hz, 2H); 3.20 (s, 1H); 2.63 (t, J=7.8 Hz, 2H); 1.64 (m, 2H); 1.41 (m, 2H); 0.97 (t, J=7.5 Hz, 3H). 13C{1H} NMR (CDCl3): 143.8, 132.1, 11.6, 131.4, 1128.6, 124.1, 121.6, 120.0, 911.7, 88.2, 83.4, 78.8, 35.6, 33.4, 22.2, 14.0 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703388B2
Source datasetuspto-grants-2014_04
ORD IDord-46308107442f4c5c835c82a6d63cdb95
Source noteuspto-grants-2014_04