HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 67491521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | HCID 21348356 | HCID 21348356 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 67491521 | HCID 67491521 | — |
Reaction Steps
To a solution of 0.398 g (2 mmol) 1-ethoxy-2,2,6,6-tetramethyl-piperidin-4-one in dry acetonitrile is added 0.297 g (3 mmol) trimethylsilyl cyanide and a catalytic amount of iodine. The solution is stirred at rt over night. The reaction mixture is extracted with ethyl acetate, washed with Na2CO3 solution and brine. The organic layer is separated, dried over Na2SO4, filtered and the solvent is removed under reduced pressure. A yellow oil was obtained and subsequently subjected to flash chromatography on silica gel using 4:1 hexane/ethyl acetate as eluent. The product was obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045480B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-454a91bde92643fa9bd4a11734581294 |
| Source note | uspto-grants-2015_06 |