HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Ethynylphenyl)(4-fluorophenyl)methanol → (4-Ethynylphenyl)(4-fluorophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Ethynylphenyl)(4-fluorophenyl)methanol | HCID 86661773 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (4-Ethynylphenyl)(4-fluorophenyl)methanone | HCID 23352815 | — |
Reaction Steps
The product of Step C was dissolved in anhydrous dioxane (20 ml) and to it MnO2 (0.5 g) was added. The suspension was stirred at reflux for 6 h and then filtered through Celite. The filtrate was distilled off and the residue was purified by FCC (SiO2) to give the product (0.18 g; 89%), as creamy paste. 1H-NMR (CDCl3) 3.24 (s, 1H); 7.15 (tr, 2H, J=8.73 Hz); 7.60 (d, 2H, J=6.69 Hz); 7.71 (d, 2H, J=6.58 Hz); 7.78-7.84 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181182B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-a3f58eee58ab42aaa2844e2f227e4cea |
| Source note | uspto-grants-2015_11 |