HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(3-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole | HCID 10881551 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide | HCID 11732904 | 90.6% |
Reaction Steps
A mixture of 4-(3-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (8.00 g), N-hydroxyphthalimide (4.13 g), potassium carbonate (7.05 g) and N,N-dimethylforrnamide (80 ml) was stirred at room temperature for 20 hours and water (800 ml) was added. The resultant crystals were filtered and washed with water to obtain N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide (10.1 g, yield 90%) as pale-brown crystals. m.p. 146-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495581B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-5c09e25e39894f9c829473abcc3f91dc |
| Source note | uspto-grants-2002_12 |