HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 662052Generated: November 1, 2026
Potassium Carbonate → HCID 178425614, compound
https://huagongshe.com/reaction/662052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 57813462 | HCID 57813462 | — |
| Reactant | HCID 67006324 | HCID 67006324 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178425614 | HCID 178425614 | 72.4% |
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 cooling to room temperature, the solvent was removed under reduced pressure. The residue was dissolved in CH2Cl2 (50 mL), 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 chomatography, eluting with CH2Cl2 to yield the captioned product (2.6 g, yield: 60%). 1H NMR (400 MHz, CDCl3) δ 0.12 (s, 6H), 0.95 (s 9H), 1.46 (s, 9H), 4.41-4.42 (m, 2H), 4.81 (s, 2H), 7.37-7.47 (m, 6H), 7.71 (d, J=8.0 Hz, 1H); 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084449B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-482b9d91321e4b7794c858335bef85fa |
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| Source note | uspto-grants-2011_12 |
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