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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657354Generated: October 28, 2026

Potassium Carbonate → HCID 86633355, compound

https://huagongshe.com/reaction/657354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant[3-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]boronic acidHCID 57813382—
ReactantHCID 86633348HCID 86633348—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86633355HCID 8663335572%

Reaction Conditions

Temperature70 °C

Reaction Steps

1,1-Dimethylethyl[(3-bromo-5-cyanophenyl)methyl]carbamate (1.90 g, 6.11 mmol), Pd(OAc)2 (76 mg), PPh3 (228 mg) and K2CO3 (1.27 g, 9.16 mmol) were dissolved in dioxane (50 mL). The mixture was heated at 70° C. for 30 min, and then [3-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]boronic acid (2.11 g, 7.94 mmol) was added. The mixture reaction was stirred at reflux overnight. The solvent was removed under reduced pressure, then the residue diluted with CH2Cl2 (100 mL). The organic layer was washed with water (30 mL) and brine (30 mL), and dried over Na2SO4. The product, 1,1-dimethylethyl{[5-cyano-3′-({[dimethyl(1-methylethyl)silyl]oxy}methyl)-3-biphenylyl]methyl}carbamate-ethane was purified by flash column chomatography (2.0 g, yield: 72%). 1H NMR (400 MHz, CDCl3) δ 0.12 (s, 6H), 0.96 (s, 9H), 1.47 (s, 9H), 4.41 (d, J=6 Hz, 2H), 4.81 (s, 2H), 7.38-7.44 (m, 3H), 7.50 (s, 1H), 7.55 (s, 1H), 7.70 (s, 1H), 7.75 (s, 1H); 13C NMR (100 MHz, CDCl3) δ −5.2, 18.4, 25.9, 28.3, 43.4, 64.7, 80.1, 113.1, 118.7, 124.7, 125.6, 126.1, 129.0, 129.2, 129.6, 130.4, 133.4, 134.8, 138.6, 141.2, 142.5, 142.9, 155.9; HPLC: retention time: 4.670 min; purity: 94.4%; MS m/z 453 (M+, 32), 339 (M+-TBS, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-205ad3e3e31b40dab7db4c5a19061235
Source noteuspto-grants-2011_12