HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → HCID 14695612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 14695585 | HCID 14695585 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14695612 | HCID 14695612 | 65% |
Reaction Steps
To an acetonitrile solution (30 ml) of 3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (0.72 g, 2.5 mmol) was added sodium carbonate (0.16 g), and the mixture was heated at reflux for 1 hour. After the addition of propargyl bromide (0.36 g, 3.0 mmol), the reaction mixture was further refluxed for 1 hour. After the solution was quenched with 0.1N hdyrochloric acid, the product was extracted with chloroform. The extracts combined were dried and evaporated as small a volume as possible. The resulting pale yellow oil was purified by silica gel column chromatography to give pure 3-(2'-fluoro-4'-chloro-5'-propargyloxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione. (0.53 g, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983751 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-6eac2ddc3eb24808b337153d5d775f9c |
| Source note | uspto-grants-1991_01 |