HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68511Generated: October 29, 2026
Hydrochloric Acid → 2-(3-Phenylbenzoyl)benzoic acid
https://huagongshe.com/reaction/68511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-(3-Bromophenyl)naphthalene | HCID 23080773 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(3-Phenylbenzoyl)benzoic acid | HCID 67065530 | 80.1% |
Reaction Steps
Under an argon atmosphere, 132 g of magnesium were dispersed in 500 mL of ether. A solution of 142 g of 2-(3-bromophenyl)naphthalene in 500 mL of ether was added to the dispersion, and then the mixture was stirred at room temperature for 1 hour. A solution of 74 g of phthalic anhydride in 150 mL of benzene was added to the mixture, and then the resultant reaction solution was stirred for 3 hours under reflux. After having been cooled to room temperature, the reaction solution was poured into ice water, and then 1 L of 10% hydrochloric acid was added to the mixture. The organic layer was separated and extracted with an aqueous solution of potassium carbonate. The alkaline extract was acidified, and then the resultant solid was washed with boiling water. The resultant crude product was recrystallized with acetic acid. Thus, 121 g of 2-(3-phenylbenzoyl)benzoic acid were obtained (in 69% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822041B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-867fba6a5611462b9e466734b4889879 |
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| Source note | uspto-grants-2014_09 |
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