HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459175Generated: October 29, 2026
Acetone → 4-[(Prop-2-en-1-yl)oxy]-1,1'-biphenyl
https://huagongshe.com/reaction/459175
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Product | 4-[(Prop-2-en-1-yl)oxy]-1,1'-biphenyl | HCID 257986 | — |
Reaction Steps
To a solution of 4-phenylphenol (1 eq) in acetone, K2CO3 (2 eq) and alkyl bromide (1.2 eq) were added and the mixture reaction was stirred at 55° C. overnight. Quenched with water and extracted with ethyl acetate. The organic layer was dried (MgSO4) and concentrated to give 4-allyloxybiphenyl. This crude product was dissolved in Me2NPh and heated to reflux for 6 hours and then stirred at room temperature over 3 days. Refluxed again for 8 hours and then poured into and ice-cold HCl 1M solution, extracted with ethyl acetate and washed with water. Dried and concentrated to give a crude product which was purified by chromatography to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192982B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-878d0cf0f3354885bd4f201d046954ab |
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| Source note | uspto-grants-2007_03 |
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