HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → HCID 15158218, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 15158214 | HCID 15158214 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15158218 | HCID 15158218 | 54% |
Reaction Steps
The product of Example J (1.6 g, 0.006 mole) was dissolved in 30 mls of dry DMF at room temperature under a nitrogen atmosphere and potassium t-butoxide (1.4 g) was added. After stirring for 5 minutes, 1 g of allyl iodide was added and the reaction was warmed to +50° C. for 1 hour. Another half equivalent of allyl iodide was added and the stirring was continued for 2 hours at +50° C. After cooling to room temperature the mixture was poured into 50 mls of 0.5N KHSO4 and extracted with ethyl acetate. After drying the organic layer over Na2SO4, the solvent was removed and the residue was chromatographed on silica gel using 10% ethyl acetate/hexane to give 1 g of the title compound (54% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04988707 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-44c833bdf1fc4ee2a55b3c16d09ff92b |
| Source note | uspto-grants-1991_01 |