HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Hydroxyacetophenone → 1-(4-((5-(Cyclohexylsulfonyl)-2-pyridinyl)oxy)phenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,5-Bis(cyclohexylsulfonyl)pyridine | HCID 13102682 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-((5-(Cyclohexylsulfonyl)-2-pyridinyl)oxy)phenyl)ethanone | HCID 13102712 | 31% |
Reaction Steps
To 3.68 g of p-hydroxyacetophenone in a 25 ml THF/25 ml DMSO mixture was added 3.2 g of t-BuOK and then 10.03 g of 2,5-bis(cyclohexylsulfonyl)pyridine, and the resulting mixture was heated at 62° C. for 11/2 hrs. The reaction mixture was cooled overnight, then added to 4 volumes of water and the crude product which formed recovered by filtration. Recrystallization of the crude product from CH2Cl2 /ethanol gave the product, 1-(4-((5-(cyclohexylsulfonyl)-2-pyridinyl)oxy)phenyl)ethanone, (31% yield), as light yellow prisms, m.p. 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616087 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-1bde1444ca8d457495e8c0d8de371dcd |
| Source note | uspto-grants-1986_10 |