HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533571Generated: October 29, 2026
Sodium Carbonate → 4-(4-Fluorophenyl)phenethyl alcohol
https://huagongshe.com/reaction/533571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Fluorophenyl)phenethyl alcohol | HCID 2759131 | — |
Reaction Steps
To a 2-5 mL microwave vial was added 2-(4-bromophenyl)ethanol (603 mg, 3.0 mmol), (4-fluorophenyl)boronic acid (462 mg, 3.3 mmol), sodium carbonate (973 mg, 9.0 mmol), palladium acetate (33.7 mg, 0.15 mmol), 1,4dioxane (4.5 mL) and water (4.5 mL). The mixture was irradiated in a CEN microwave at 120° C. for 10 minutes. The reaction mixture was biphasic upon reaction completion. The reaction mixture was extracted into ethyl acetate (2×150 mL) dried over Na2SO4 then filtered through a pad of celite. The organics were concentrated in vacuo and the crude material was purified by chromatography on silica gel (gradient: 70:30 heptanes:EtOAc). Isolated material still contained 2-(4-bromophenyl)ethanol, therefore, the material was triturated in heptanes to furnish the title compound as a white solid. (430 mg, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853258B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-6cb0a834f34b46cf8b228c5a983cf3cf |
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| Source note | uspto-grants-2014_10 |
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