HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 15578417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | HCID 15578433 | HCID 15578433 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15578417 | HCID 15578417 | — |
Reaction Steps
A solution of bromide (10.25 ml, 0.198 mol) in chloroform (50 ml) was added dropwise over 30 minutes to a stirred solution of ethyl 6-phenyl-2,4,6-trioxohexanoate (52.0 g) in chloroform (400 ml) at -10 to -20° C. The pale solution was stirred for a further 3 hours without cooling, washed with water and evaporated. The residual solid was recrystallised from ethanol-water to give ethyl 3-bromo-4-oxo-6-phenyl-4H-pyran-2-carboxylate (mp 135° C.). This ester was hydrolysed as in Example 33 to give the title product (mp 247° C. with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04471129 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-fd0c84017f964230b81a112ce1ad34bc |
| Source note | uspto-grants-1984_09 |