HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2,6-Diphenylphenoxyethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | 2,6-Diphenylphenol | HCID 75512 | — |
| Reactant | Acrylic acid 4-[1,1-bis-(4-acryloyloxy-phenyl)-ethyl]-phenyl ester | HCID 11568972 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,6-Diphenylphenoxyethanol | HCID 68976121 | — |
Reaction Steps
To a 50 ml 1 neck round bottom was added 2,6-diphenylphenol (10 g, 1 eq), ethylene carbonate (3.9 g, 1.1 eq), potassium iodide (0.07 g, 0.01 eq), dimethylformamide (1 g, 0.3 eq) and heated to 150 C. After 4 hours the reaction was cooled to 40 C, added 30 ml ethyl acetate and washed 2 times with 20 ml sodium chloride brine, 3 times with 20 ml DI water and again with 20 ml brine. The ethyl acetate was dried with (1 g) magnesium sulfate, filtered and concentrated invacuo to recover an off-white solid. Mp 77-78
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586154B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-42ed4df8c97a437195be52eb1ca968ae |
| Source note | uspto-grants-2013_11 |