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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 662060Generated: November 2, 2026

Potassium Phosphate, Tribasic → 1,1-Dimethylethyl {[3'-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-5-(methyloxy)-3-biphenylyl]methyl}carbamate

https://huagongshe.com/reaction/662060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(1R)-Dicyclohexyl(2'-methoxy-[1,1'-binaphthalen]-2-yl)phosphaneHCID 16079156—
Reactant[3-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]boronic acidHCID 57813382—
ReactantTert-butyl 3-bromo-5-methoxybenzylcarbamateHCID 57813417—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product1,1-Dimethylethyl {[3'-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-5-(methyloxy)-3-biphenylyl]methyl}carbamateHCID 5781327474%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1-dimethylethyl {[3-bromo-5-(methyloxy)phenyl]methyl}carbamate (1.4 g, 4.43 mmol), Pd(OAc)2 (70.0 mg, 0.14 mmol), dicyclohexyl[2′-(methyloxy)-1,1′-binaphthalen-2-yl]phosphane (84.0 mg, 0.175 mmol) and K3PO4 (1.2 g, 5.31 mmol) were dissolved in dioxane (30 mL). The mixture was heated at 80° C. for 30 min, and then [3-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]boronic acid (1.5 g, 5.76 mmol) was added. The mixture reaction was stirred at reflux for two days. The solvent was removed under reduced pressure, then the residue diluted with CH2Cl2 (100 mL). The organic layer was washed with water (20 mL), brine (20 mL), and dried over Na2SO4. The product 1,1-dimethylethyl[3′-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-5-(methyloxy)-3-biphenylyl]methyl}carbamate (1.5 g) was purified by flash column chomatography (PE:EA=15:1) (yield: 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084449B2
Source datasetuspto-grants-2011_12
ORD IDord-23d386f1e07b4e89a6a3442dace46d65
Source noteuspto-grants-2011_12