HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenacyl bromide → HCID 57222157, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 103187-09-3 | HCID 18397185 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 57222157 | HCID 57222157 | 99% |
Reaction Steps
A mixture of (7R)-(+)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoic acid (0.71 g, 2.0 mmoles), p-bromophenacylbromide (0.56 g, 2.0 mmoles), and potassium carbonate (0.30 g, 2.2 mmole) in acetone (15 ml) was stirred for 2.5 hours at room temperature. After the reaction was completed, the solvent was evaporated in a reduced pressure, the residue was taken up in the isopropylether. Working up in the usual manner gave the crude product, which was chromatographed on silica gel column with isopropylether to give p-bromophenacyl (7R)-(+)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoate (1.09 g, 99%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05304658 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-65b75f8a374d4770ac90d3b6f986b6b0 |
| Source note | uspto-grants-1994_04 |