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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037401Generated: October 26, 2026

Potassium Carbonate → {1-[4-(8-ethynyl-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1037401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(1-[4-(4-oxo-2-phenyl-8-trimethylsilanylethynyl-4H-chromen-3-yl)-phenyl]-cyclobutyl)-carbamic acid tert-butyl esterHCID 67067912—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product{1-[4-(8-ethynyl-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl esterHCID 86671055100.6%

Reaction Steps

A solution of {1-[4-(4-oxo-2-phenyl-8-trimethylsilanylethynyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester (51 mg, 0.091 mmol) in MeOH (2 mL) and DCM (1 mL) was treated with potassium carbonate (15 mg, 0.109 mmol) and the reaction stirred at RT for 3 h. The reaction mixture was quenched with water, diluted with EtOAc, washed with brine, dried (Na2SO4), filtered and concentrated in vacuo to give the title compound as a foamy solid (45 mg, 100%). 1H NMR (400 MHz, CDCl3): δ 8.27 (dd, J=7.7 and 1.6 Hz, 1H), 7.86 (dd, J=7.5 and 1.6 Hz, 1H), 7.48 (d, J=7.5 Hz, 2H), 7.41-7.30 (m, 5H), 7.25-7.19 (m, 3H), 5.06 (s, 1H), 3.47 (s, 1H), 2.65-2.27 (m, 4H), 2.14-2.00 (m, 1H), 1.91-1.76 (m, 1H), 1.37 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-2f09974c9cdf40fdbab82aeb9e8040ab
Source noteuspto-grants-2013_10