HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852489Generated: October 31, 2026
Potassium Carbonate → HCID 86689303, compound
https://huagongshe.com/reaction/1852489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Aminobenzonitrile | HCID 16702 | — |
| Reactant | HCID 86689304 | HCID 86689304 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86689303 | HCID 86689303 | 86.1% |
Reaction Steps
An anhydrous toluene (30 mL) suspension of 1-nitro-5,6,7,8-tetrahydronaphthalen-2-yl triflate (1.95 g, 6.00 mmol), 3-aminobenzonitrile (1.06 g, 9.00 mmol), potassium carbonate (830 mg, 6.00 mmol), tetrakis(triphenylphosphine)palladium (346 mg, 0.30 mmol), and triphenylphosphine (158 mg, 0.60 mmol) was stirred at 110° C. for 18 hours. The reaction mixture was cooled on standing, and filtered. The filtrate was diluted with ethyl acetate. The obtained organic solution was washed with purified water, and dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (chloroform) to give the titled compound as orange powder (1.515 g, yield 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962613B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-3cb108f9fb234edaa689835b2f26916f |
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| Source note | uspto-grants-2015_02 |
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