HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442277Generated: October 30, 2026
Allyl bromide → Methyl-2-allyloxy-5-(4'-fluorophenyl)-benzoate
https://huagongshe.com/reaction/442277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4'-fluoro-4-hydroxy-[1,1'-biphenyl]-3-carboxylate | HCID 21416429 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl-2-allyloxy-5-(4'-fluorophenyl)-benzoate | HCID 21416435 | — |
Reaction Steps
A mixture of 6.6 g. of methyl-5-(4'-fluorophenyl)-2-hydroxy-benzoate, 5.5 g. of potassium carbonate, 25 ml. of acetone, and 4.5 g. of allyl bromide is heated at reflux for 2 hours, and then stirred at 25° C. overnight. The reaction mixture is partitioned between 100 ml. of water and 100 ml. of ether, the ether solution is dried over magnesium sulfate and concentrated to a thick oil, 6.0 g. This material shows a strong absorption band in the infra-red at 5.75 μ (non-bonded ester) and is homogeneous by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04044049 |
|---|
| Source dataset | uspto-grants-1977_08 |
|---|
| ORD ID | ord-c3c12bcc81d7431784eea7e866879232 |
|---|
| Source note | uspto-grants-1977_08 |
|---|