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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825787Generated: October 31, 2026

Potassium Carbonate → HCID 22139398, compound

https://huagongshe.com/reaction/1825787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-morpholinopyran-4-oneHCID 6605262—
ReactantHCID 67524621HCID 67524621—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22139398HCID 2213939818.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

Carbonic acid tert-butyl ester 1-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-9H-thioxanthen-4-yl ester (3.00 g, 6.81 mmol), 2-chloro-6-morpholin-4-yl-pyran-4-one (1.22 g, 5.67 mmol) and potassium carbonate (2.07 g, 14.98 mmol) were suspended in anhydrous dioxane (6 ml) under nitrogen atmosphere. The solution was degassed for 15 minutes. To the solution tetrakis(triphenylphosphino) palladium (291 mg, 5% eq.) was added. The mixture was degassed for a further 5 minutes. The reaction was heated at 90° C. under nitrogen atmosphere for 24 hours. The solvent was evaporated in vacuo and the crude mixture was purified by column chromatography (9:1, ethyl acetate/ethanol), to yield the title compound (421 mg, 16%) as a light yellow amorphous solid. 1H NMR (300 MHz, DMSO-d6): δH=3.33 (4H, t), 3.67 (4H, t), 3.88 (2H, s), 5.45 (1H, d), 6.05 (1H, d), 6.87 (1H, d), 7.24–7.65 (5H, m), 10.62 (1H, bs); m/z (LC-MS, ESP), RT=3.96 min, (M++1)=394.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049313B2
Source datasetuspto-grants-2006_05
ORD IDord-e3a02019fa214321886f8d3a628d4670
Source noteuspto-grants-2006_05