HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 15582984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 13503453 | HCID 13503453 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15582984 | HCID 15582984 | — |
Reaction Steps
A mixture of 2.11 g. of N-[4-bromo-3-(1-carboxybutyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide, 11.19 g. of phenacyl bromide, 0.64 g. of potassium fluoride and 10 ml. of acetonitrile was refluxed with stirring for 8.5 hours and the reaction mixture was cooled and the precipitate was separated by a filtration. The filtrate was concentrated under a reduced pressure and the residue was purified by a chromatography on a column of silica gel (developing solvent of benzene) to obtain 2.20 g. of Compound No. 141 shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536209 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-f90509e0c3714a23bf2e730e67be18ed |
| Source note | uspto-grants-1985_08 |