HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 17861229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 2,4-Dihydroxybenzophenone | HCID 8572 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chloromethylphenoxy)methyl-5-methyl-2-phenyloxazole | HCID 10946940 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 17861229 | HCID 17861229 | 40% |
Reaction Steps
A mixture of 4-(4-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole-(2.76 g), 2,4-dihydroxybenzophenone (2.00 g), anhydrous potassium carbonate (1.29 g) and acetone (50 mL) was heated under reflux for 0.15 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated to give crystals (1.72 g, 40%) of 4-[4-(4-benzoyl-3-hydroxyphenoxymethyl)phenoxymethyl]-5-methyl-2-phenyloxazole. Recrystallization from ethyl acetate-hexane gave pale-yellow prism crystals. melting point: 160-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-156568e1916e44f2addf5a31f2e2d489 |
| Source note | uspto-grants-2007_07 |