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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673013Generated: October 30, 2026

Potassium Carbonate → 1-Ethynyl-3-methanesulfonylbenzene

https://huagongshe.com/reaction/1673013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant[2-(3-Methanesulfonylphenyl)ethynyl]trimethylsilaneHCID 59240077—
SolventMethanolHCID 887—
Product1-Ethynyl-3-methanesulfonylbenzeneHCID 20515145—

Reaction Steps

The TMS-acetylene 1.58 g (626 μmol) was treated with 1.02 g of potassium carbonate and 10.0 mL of methanol. The resulting suspension was stirred at room temperature for 3 h then was concentrated to remove methanol. The residue was washed into a separatory funnel with ethyl acetate and water. The ethyl acetate was separated, washed with ammonium chloride, brine, was dried (Na2SO4), and concentrated in vacuo. The residue was purified by silica gel flash chromatography (Jones Flashmaster, 50 g Silica gel, gradient elution from 100% hexanes to 40% ethyl acetate over 30 minutes). Appropriate fractions were combined and concentrated in vacuo affording 1-Ethynyl-3-methanesulfonyl-benzene as a cream colored solid, yield: 977 mg (86.6%). 1H NMR (CDCl3): δ 8.07 (s, 1H), 7.92 (d, J=8 Hz, 1H), 7.75 (d, J=8 Hz, 1H), 7.55 (t, J=8 Hz, 1H), 3.22 (s, 1H), 3.06 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998995B2
Source datasetuspto-grants-2011_08
ORD IDord-07e83e1e57ed4aff8789e69dd95891c3
Source noteuspto-grants-2011_08