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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564472Generated: October 30, 2026

Potassium Carbonate → HCID 178439150, compound

https://huagongshe.com/reaction/564472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 57813462HCID 57813462—
ReactantHCID 67006324HCID 67006324—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178439150HCID 178439150568%

Reaction Conditions

Temperature80 °C

Reaction Steps

Pd(OAc)2 (56.3 mg, 0.25 mmol), PPh3 (263.0 mg, 1.0 mmol), K2CO3 (1.7 g, 12.5 mmol) and 1,1-dimethylethyl [(3-bromo-4-cyanophenyl)methyl]carbamate (2.6 g, 8.4 mmol) were suspended in 1,4-dioxane (30 mL). After the mixture was heated to 80° C. for 15 min, [3-(hydroxymethyl)phenyl]boronic acid-(1,1-dimethylethyl)(trimethyl)silane (2.7 g, 10.0 mmol) was added. Then the reaction mixture was stirred over night at 100° C. After cooled to room temperature, the solvent was removed under reduced pressure. The residue was dissolved in CH2Cl2 (50 mL), then washed with water (20 mL), brine (20 mL), and dried over Na2SO4. After the solvent was removed, the crude product was purified on Al2O3 column chromatography, eluting with CH2Cl2. 2.6 g of the product, 1,1-dimethylethyl{[3′-({[(1,1-dimethylethyl)(methyl)silyl]oxy}methyl)-6-methyl-3-biphenylyl]methyl}carbamate-ethane, was obtained (yield: 60%). 1H NMR (400 MHz, CDCl3): δ 0.12 (s, 6 H), 0.95 (s 9 H), 1.46 (s, 9 H), 4.41-4.42 (m, 2 H), 4.81 (s, 2 H), 7.37-7.47 (m, 6 H), 7.71 (d, J=8.0 Hz, 1 H); 13C NMR (100 MHz, CDCl3): δ −5.3, 18.4, 25.9, 28.3, 44.2, 64.7, 80.0, 109.9, 118.6, 126.1, 126.2, 126.4, 127.3, 128.6, 134.0, 137.9, 142.0, 144.5, 145.8, 155.8; HPLC: retention time: 9.500 min; purity: 95.2% (HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067408B2
Source datasetuspto-grants-2011_11
ORD IDord-7355885c293e4ead93893f922334027b
Source noteuspto-grants-2011_11