HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130646Generated: October 30, 2026
Phenylboronic Acid → HCID 59730978, compound
https://huagongshe.com/reaction/130646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Barium hydroxide, octahydrate | HCID 17749109 | — |
| Reactant | HCID 59730973 | HCID 59730973 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 59730978 | HCID 59730978 | 26.2% |
Reaction Steps
Next, to a mixture of 2-(3-bromophenyl)-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)acetamide (50.0 mg, 0.139 mmol), phenyl boronic acid (25.4 mg, 0.208 mmol), tri-o-tolylphosphine (8.45 mg, 0.028 mmol), and barium hydroxide octahydrate (65.7 mg, 0.208 mmol) in 12 mL of ethylene glycol dimethyl ether was added ethanol (4 mL), water (4 mL), and palladium(II) acetate (3.12 mg, 0.014 mmol). The mixture was stirred vigorously under argon and was heated to reflux. After cooled to room temperature, water was added and the product was extracted with ethylacetate. The organic layer was washed with water then brine, dried over MgSO4, filtered, and concentrated under reduced pressure to obtain 2-biphenyl-3-yl-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)acetamide (13.0 mg, 26% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381840B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-7ce1317420e94333a07f800d83d3dd10 |
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| Source note | uspto-grants-2008_06 |
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