Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | Ethyl 2-iodo-4-methyl-5-oxazolecarboxylate | HCID 12785853 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20064728 | HCID 20064728 | 57.1% |
Reaction Steps
A reaction vessel fitted with a calcium sulfate drying tube was charged with 5 ml of toluene, 0.56 g (2 mmol) of ethyl 2-iodo-4-methyl-5-oxazolecarboxylate and 2 ml (10 mmol) of dibenzylamine. The reaction mixture was stirred overnight at room temperature. The reaction mixture was then heated at reflux for 4 hours, cooled, and then diluted with ethyl ether. The mixture was washed with water, then with 5% hydrochloric acid, and then with water. The ether solution was dried with sodium sulfate and then concentrated under reduced pressure to yield 0.4 g of a yellow glass. This glass was dissolved in hot hexane and then with the vessel cooling in a dry ice bath, a white solid material was deposited. The solid material was filtered off giving 0.35 g of product (m.p.=75°-77° C.) identified in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05000775 |
|---|
| Source dataset | uspto-grants-1991_03 |
|---|
| ORD ID | ord-904f9d3177fb489fa6ec43b9aa9b5a15 |
|---|
| Source note | uspto-grants-1991_03 |
|---|