HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227866Generated: October 25, 2026
Methyl 4-chlorobenzoate → 4-Carbomethoxy-3'-Acetylbiphenyl
https://huagongshe.com/reaction/227866
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-chlorobenzoate | HCID 14307 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 3-Acetylphenylboronic acid | HCID 2734310 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Product | 4-Carbomethoxy-3'-Acetylbiphenyl | HCID 4328804 | 90.1% |
Reaction Steps
An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), 3-acetylphenyl boronic acid (246 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and methyl-4-chlorobenzoate (171 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with water (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 229 mg (90%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560582B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-bbe068dc8e8b4085bf7c87ce78ff61e9 |
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| Source note | uspto-grants-2009_07 |
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