HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227873Generated: October 25, 2026
4'-Bromoacetanilide → N-Acetyl-4-aminobiphenyl
https://huagongshe.com/reaction/227873
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Bromoacetanilide | HCID 7683 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Product | N-Acetyl-4-aminobiphenyl | HCID 19998 | 86.2% |
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, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 4′-bromoacetanilide (214 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 bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 182 mg (86%) 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-7f9e88ff24594db1b6115af7ca086cf9 |
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| Source note | uspto-grants-2009_07 |
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