HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 54155194, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Diazonio-3-oxo-1-[(prop-2-en-1-yl)oxy]but-1-en-1-olate | HCID 54170651 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54155194 | HCID 54155194 | 78.8% |
Reaction Steps
Into 5 ml of dry acetonitrile were added 167 mg (1 millimole) of allyl 2-diazoacetoacetate and 210 mg (1.4 millimoles) of sodium iodide. To the mixture were added 220 μl (1.6 millimoles) of triethylamine and then 190 μl (1.5 millimoles) of trimethylsilyl chloride while agitating under an argon atmosphere at a room temperature. After the resultant was agitated at a room temperature for an hour, it was concentrated under a reduced pressure. To the residue was added 10 ml of dry hexane, and the resultant was agitated for 30 min. at a room temperature. Isoluble materials were removed by filtration and the hexane solution was concentrated to dryness under a reduced pressure to give 176 mg (yield 78.8%) of the desired compound in an oily state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071966 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-7733eaacad754abcbde5ac80cf11d5cf |
| Source note | uspto-grants-1991_12 |