HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184459Generated: October 30, 2026
Sodium Carbonate → Methyl 4-(naphthalen-1-yl)benzoate
https://huagongshe.com/reaction/2184459
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 4-bromobenzoate | HCID 12081 | — |
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-(naphthalen-1-yl)benzoate | HCID 10934276 | 97.8% |
Reaction Steps
Methyl 4-bromobenzoate (0.96 g, 4.46 mmol) was added to a mixture of 1-naphthaleneboronic acid (0.73 g, 4.25 mmol) and sodium carbonate (0.075 g, 7.08 mmol) in toluene (30 mL), ethanol (6 mL) and water (12 mL). The resultant solution was purged with nitrogen for 10 minutes before tetrakis(triphenylphosphine) palladium(0) (0.10 g, 0.09 mmol) was added. The reaction mixture was heated to reflux for 65 hours. The solution was cooled to ambient temperature, then filtered through a pad of Celite, which was subsequently rinsed with ethyl acetate. The combined filtrate was diluted to 100 mL with water/ethyl acetate (1:1, v/v). The aqueous layer was extracted with ethyl acetate, and the combined extracts were dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness to yield the title compound as a gold oil (1.09 g). This material was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900200B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-f718c57d28cc41cb84c76a30f3485482 |
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| Source note | uspto-grants-2005_05 |
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