HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 18174752, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl [(4-hydroxyphenyl)methyl]phosphonate | HCID 14519610 | — |
| Reactant | HCID 18174693 | HCID 18174693 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18174752 | HCID 18174752 | — |
Reaction Steps
3-[4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolyl]propyl methanesulfonate (400 mg), diethyl 4-hydroxybenzylphosphonate (365 mg), potassium carbonate (276 mg) and N,N-dimethylformamide (10 ml) was stirred at 100° C. for 4 hours. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (100 ml×2). The organic layer was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography, and diethyl 4-[3-[4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolyl]propyloxy]benzylphosphonate was obtained as a yellow oil (526 mg, 97%) from an ethyl acetate-eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605629B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-8b7c93446bc14ec78932f58f0c24d23b |
| Source note | uspto-grants-2003_08 |