HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 21846056, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | HCID 21846057 | HCID 21846057 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21846056 | HCID 21846056 | — |
Reaction Steps
0.24 g (1.05 mmol) of 6- cyano-4-(2-hydroxyethyl)-1-methyl-2(1H)-quinolone is added in small amounts to 0.48 g (1.14 mmol) of dibromotriphenylphosphorane in 14 ml of dichdoromethane at room temperature. After 75 minutes of stirring at room temperature, the reaction medium is poured into 200 ml of dichloromethane and the mixture is washed with water. The organic phase is dried over sodium sulphate, filtered and condensed under vacuum. The white residue is ground in diethylether. The solid obtained is taken up in a minimum of dichloromethane, the mixture is filtered rapidly through a layer of silica, eluting with ether, and the filtrate is evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958924 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-676df577da584d96b58a1146095ef8b2 |
| Source note | uspto-grants-1999_09 |