HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 67343897, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 136344252 | HCID 136344252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67343897 | HCID 67343897 | — |
Reaction Steps
To a mixture of 0.71 g of 4-hydroxy-3-[3-[3-(methoxycarbonylmethoxy)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone in 5 ml of dimethylformamide was added 0.09 g of sodium hydroxide (60% oily), and this was stirred at room temperature for 1 hour. 0.26 ml of allyl bromide was added, and this was stirred at room temperature overnight. The solvent was distilled off under reduced pressure, 5 ml of tetrahydrofuran was added, insolubles were filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.30 g of 4-allyloxy-3-[3-[3-(methoxycarbonylmethoxy)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone [Compound No. (1b)] as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989478B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-38ce46544811402490c4206356c858d2 |
| Source note | uspto-grants-2011_08 |