HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871819Generated: October 30, 2026
Phenyl-1-naphthylamine → HCID 22222674, compound
https://huagongshe.com/reaction/871819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl-1-naphthylamine | HCID 7013 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22222674 | HCID 22222674 | — |
Reaction Steps
4-Bromobenzaldehyde (1.00 g, 5.40 mmol), 1-anilinonaphthalene (1.42 g, 6.48 mmol) and Pd(OAc)2 (25 mg, 0.11 mmol) and NaOtBu (623 mg, 6.48 mmol) were charged in a sealed tube. The sealed tube was deoxygenated and purged with nitrogen, and added dried o-xylene (30 mL) and tri-tert-butylphosphine (0.23 ml, 0.11 mmol). The reaction was heated to 120° C., and stirred for 48 hours. The resulting was filtered to remove metal and then concentrated under reduced pressure and the residue was purified by column chromatography (hexanes/CH2Cl2=1/1) to afford F (1.10 g, 63%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08974920B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-281b3d5fcf384895a9d1828515937d9f |
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| Source note | uspto-grants-2015_03 |
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