HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 6-(4-Pentylphenyl)-1-chloro-2-naphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-Bromo-1-chloronaphthalen-2-ol | HCID 22048159 | — |
| Reactant | 4-Pentylphenylboric acid | HCID 23450917 | — |
| Reactant | Ethanol toluene water | HCID 86587398 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(4-Pentylphenyl)-1-chloro-2-naphthol | HCID 59264278 | 78.1% |
Reaction Steps
At first, 55 g of 6-bromo-1-chloro-2-naphthol (S1-2), 12.3 g of 4-pentyl-phenylboric acid (S1-3), 1.0 g of tetrakis(triphenylphosphine) palladium, 13.6 g of sodium carbonate and 100 ml of a mixed solvent of toluene/ethanol/water=3/3/1 were added to a reactor in nitrogen atmosphere and refluxed for 10 hours. The reaction solution was cooled to room temperature, added with toluene, and then washed with 1N HCl(aq) and water, dried over magnesium sulfate and distilled under a reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography using toluene as an eluting solvent, and then dried under a reduced pressure to obtain 15 g of 6-(4-pentylphenyl)-1-chloro-2-naphthol (S1-4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07727417B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-ecfb716693ae4e1b944330ff514b9b38 |
| Source note | uspto-grants-2010_06 |