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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456034Generated: October 30, 2026

Potassium Carbonate → HCID 59187023, compound

https://huagongshe.com/reaction/456034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 24959215HCID 24959215—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
ProductHCID 59187023HCID 59187023—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(2,3-Bis-allyloxy-4-methoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanone from example 6 (3.9 g, 9.55 mmol) was dissolved in MeOH (96 mL) and cooled to 0° C. under argon. Pd(PPh3)4 (110 mg, 0.0955 mmol) was added followed by K2CO3 (1.3 g, 9.55 mmol). The cooling bath was removed and the reaction mixture was stirred for 3 hours and then evaporated in vacuo. The crude was redissolved in EtOAc (100 mL) and washed twice with NH4Cl (sat, 50 mL). The organic phase was dried over Na2SO4 and evaporated in vacuo and purified by flash chromatography using a gradient of toluene and 2% EtOAc as eluent. 1-(3-Allyloxy-2-hydroxy-4-methoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanone was obtained as a white solid. 1H NMR (CDCl3) δ=11.90 (1H, s), 8.53 (2H, s), 7.68 (1H, d), 6.58 (1H, d), 6.10 (1H, m), 5.26 (2H, m), 4.66 (2H, s), 4.59 (2H, d), 3.96 (3H, s). Yield 2.2 g (64%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497380B2
Source datasetuspto-grants-2013_07
ORD IDord-764fbcb510a144dcb75ef0ffe26f7267
Source noteuspto-grants-2013_07